Variant report

Variant	nsv1015688
Chromosome Location	chr7:104849770-105182998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5632)
CpG islands
(count:4581)
Chromatin interactive
region (count:406)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:5632 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104924529-104924792	K562	blood:	n/a	n/a
2	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
4	ARID3A	chr7:104909503-104909771	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:104909404-104910342	K562	blood:	n/a	chr7:104910069-104910085 chr7:104909863-104909879 chr7:104909862-104909878
6	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
9	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
10	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
11	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
13	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
14	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
15	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
16	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
17	ARID3A	chr7:104873284-104873810	K562	blood:	n/a	n/a
18	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
19	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
20	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
21	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
22	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
23	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
24	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
25	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
26	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
27	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
28	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
29	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
30	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
31	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
32	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
33	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
34	ARID3A	chr7:104897645-104898076	K562	blood:	n/a	n/a
35	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
36	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
37	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
38	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
39	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
40	ATF1	chr7:104908668-104908848	K562	blood:	n/a	n/a
41	ATF1	chr7:104902188-104902552	K562	blood:	n/a	n/a
42	ATF1	chr7:104897219-104897309	K562	blood:	n/a	n/a
43	ATF1	chr7:104865550-104866001	K562	blood:	n/a	n/a
44	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
45	ATF1	chr7:104897712-104898056	K562	blood:	n/a	n/a
46	ATF2	chr7:104992448-104993159	GM12878	blood:	n/a	n/a
47	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a
48	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF2	chr7:105172257-105172894	GM12878	blood:	n/a	n/a
50	ATF2	chr7:105171988-105172822	GM12878	blood:	n/a	n/a

(count:4581 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:104879299-104879349	SK-N-SH_RA	brain:	n/a
2	chr7:105162878-105162928	HepG2	liver:	n/a
3	chr7:105029499-105029549	AG10803	skin:	n/a
4	chr7:105172664-105172714	Jurkat	blood:	n/a
5	chr7:105162855-105162905	HRE	kidney:	n/a
6	chr7:104869132-104869182	Hepatocyte	liver:	n/a
7	chr7:104879299-104879349	SK-N-SH_RA	brain:	n/a
8	chr7:105162878-105162928	HepG2	liver:	n/a
9	chr7:105029499-105029549	AG10803	skin:	n/a
10	chr7:105172664-105172714	Jurkat	blood:	n/a
11	chr7:105162855-105162905	HRE	kidney:	n/a
12	chr7:104869132-104869182	Hepatocyte	liver:	n/a
13	chr7:105079663-105079713	AG04449	skin:	fetal
14	chr7:105172974-105173024	HCM	heart:	n/a
15	chr7:104885375-104885425	LNCaP	prostate:	n/a
16	chr7:105162577-105162627	SAEC	small airway:	n/a
17	chr7:105165592-105165642	AoSMC	blood vessel:	n/a
18	chr7:105029499-105029549	AG04450	lung:	fetal
19	chr7:105110948-105110998	HCPEpiC	choroid plexus:	n/a
20	chr7:105029497-105029547	PrEC	prostate:	n/a
21	chr7:105161983-105162033	AG09319	gingival:	n/a
22	chr7:104879299-104879349	ovcar-3	ovarian:	n/a
23	chr7:104945248-104945298	NH-A	brain:	n/a
24	chr7:104943515-104943565	AG10803	skin:	n/a
25	chr7:104885108-104885158	BE2_C	brain:	n/a
26	chr7:105165592-105165642	BE2_C	brain:	n/a
27	chr7:104941977-104942027	BJ	skin:	n/a
28	chr7:104888858-104888908	MCF10A-Er-Src	breast:	n/a
29	chr7:105030168-105030218	PrEC	prostate:	n/a
30	chr7:105029895-105029945	GM12878	blood:	n/a
31	chr7:104939819-104939869	NB4	blood:	n/a
32	chr7:104994322-104994372	RPTEC	kidney:	n/a
33	chr7:104994322-104994372	SK-N-SH	brain:	n/a
34	chr7:104981497-104981547	AG09309	skin:	n/a
35	chr7:104869288-104869338	GM12892	blood:	n/a
36	chr7:105128488-105128538	MCF-7	breast:	n/a
37	chr7:105176805-105176855	AG04450	lung:	fetal
38	chr7:105170241-105170291	GM06990	blood:	n/a
39	chr7:105030168-105030218	NB4	blood:	n/a
40	chr7:105161983-105162033	SAEC	small airway:	n/a
41	chr7:104945248-104945298	NHDF-neo	bronchial:	n/a
42	chr7:104865796-104865846	T-47D	breast:	n/a
43	chr7:105172168-105172218	HUVEC	blood vessel:	n/a
44	chr7:104909815-104909865	HCT-116	colon:	n/a
45	chr7:105172520-105172570	Hela-S3	cervix:	n/a
46	chr7:105172168-105172218	AG09319	gingival:	n/a
47	chr7:105162878-105162928	AG09309	skin:	n/a
48	chr7:104981497-104981547	H1-hESC	embryonic stem cell:	embryo
49	chr7:105172722-105172772	SAEC	small airway:	n/a
50	chr7:105028539-105028589	RPTEC	kidney:	n/a

(count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Distal block	Cell Line	Cell type
1	chr7:105160711..105163604-chr7:105655467..105658687,3	K562	blood:
2	chr7:104981388..104983616-chr7:105078711..105081522,2	MCF-7	breast:
3	chr7:104653151..104655346-chr7:105160083..105164134,5	K562	blood:
4	chr7:105029824..105032086-chr7:105067490..105069979,2	K562	blood:
5	chr7:104861681..104863242-chr7:104872431..104874616,2	K562	blood:
6	chr7:104864938..104867241-chr7:104867879..104870471,2	K562	blood:
7	chr7:105152955..105155476-chr7:105155749..105158829,5	K562	blood:
8	chr7:104652684..104654686-chr7:105018290..105019897,2	K562	blood:
9	chr7:104837867..104839378-chr7:104977960..104980667,2	MCF-7	breast:
10	chr7:104966725..104970068-chr7:104975373..104978585,3	MCF-7	breast:
11	chr7:105111430..105113380-chr7:105117315..105120062,2	K562	blood:
12	chr7:104902229..104905190-chr7:104911272..104913681,2	MCF-7	breast:
13	chr7:105148994..105150495-chr7:105172517..105174104,2	MCF-7	breast:
14	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
15	chr7:105139837..105141467-chr7:105172365..105173927,2	K562	blood:
16	chr7:105041786..105042328-chr7:105128303..105129103,3	MCF-7	breast:
17	chr7:104851794..104856140-chr7:104862639..104865713,4	K562	blood:
18	chr7:105069108..105071061-chr7:105077063..105078737,2	MCF-7	breast:
19	chr7:105160687..105164718-chr7:105170642..105174239,14	MCF-7	breast:
20	chr7:104649355..104651089-chr7:105173782..105176536,2	K562	blood:
21	chr7:105069185..105071026-chr7:105110310..105112272,2	MCF-7	breast:
22	chr7:105090469..105092100-chr7:105095217..105096775,2	MCF-7	breast:
23	chr7:104902229..104905190-chr7:104911272..104913681,2	MCF-7	breast:
24	chr7:104841876..104843481-chr7:104848260..104849927,2	MCF-7	breast:
25	chr7:105162231..105163027-chr7:105172004..105172750,2	K562	blood:
26	chr7:105128652..105130431-chr7:105155897..105157484,2	MCF-7	breast:
27	chr7:105065275..105067790-chr7:105068952..105071449,2	K562	blood:
28	chr7:105069861..105070836-chr7:105128119..105128880,2	MCF-7	breast:
29	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
30	chr7:105139311..105141593-chr7:105161601..105163492,2	K562	blood:
31	chr7:104924058..104925048-chr7:104956656..104957758,5	MCF-7	breast:
32	chr7:104523873..104524762-chr7:104976177..104976740,2	K562	blood:
33	chr7:105111430..105113564-chr7:105117315..105119361,2	K562	blood:
34	chr7:104860454..104863206-chr7:104876293..104878733,2	K562	blood:
35	chr7:104924217..104925131-chr7:104956599..104958078,10	MCF-7	breast:
36	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
37	chr7:104996114..104998066-chr7:105006500..105008822,2	K562	blood:
38	chr7:105027873..105030289-chr7:105032532..105034391,3	MCF-7	breast:
39	chr7:104867894..104871932-chr7:104875141..104878987,5	K562	blood:
40	chr7:104772977..104775390-chr7:105160456..105162601,2	K562	blood:
41	chr7:105147334..105150075-chr7:105152769..105155658,2	K562	blood:
42	chr7:104924058..104925116-chr7:104956648..104957763,18	MCF-7	breast:
43	chr7:105115487..105117775-chr7:105123011..105125006,2	K562	blood:
44	chr7:105171303..105174411-chr7:105176077..105181251,7	MCF-7	breast:
45	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
46	chr7:104956419..104959017-chr7:104967499..104969539,3	MCF-7	breast:
47	chr7:104652025..104655487-chr7:105171171..105176319,6	K562	blood:
48	chr20:49308527..49309123-chr7:104935923..104936615,2	MCF-7	breast:
49	chr7:104862522..104864551-chr7:104866607..104868300,2	K562	blood:
50	chr7:104955875..104958627-chr7:104961394..104962913,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-5	chr7:104909253-104909316	NONHSAT122614
2	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623
3	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
4	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614
5	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
6	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
7	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1
8	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
9	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623
10	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
11	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PUS7	hsa-miR-32-5p	chr7:105098074-105098095
2	PUS7	hsa-miR-155-5p	chr7:105097684-105097705

Variant related genes	Relation type
ENSG00000213361	TF binding region
RINT1	TF binding region
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
ENSG00000223886	TF binding region
PUS7	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
ENSG00000213361	CpG island
RINT1	CpG island
RWDD4P1	CpG island
RNU6-1322P	CpG island
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000091127	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000272604	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000271482	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000213361	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000231167	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000244490	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000223473	chromatin interactions

Extended variants
information (count: 13177 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:13177 , 50 per page) page: 1 2 3 4 5 6 7 ... 264

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533755018	chr7:104849788-104849789	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs74606324	chr7:104849834-104849835	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186252090	chr7:104849851-104849852	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570979446	chr7:104849879-104849880	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542871094	chr7:104849905-104849906	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562621801	chr7:104849918-104849919	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs141610847	chr7:104849941-104849942	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544994413	chr7:104850009-104850010	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565050935	chr7:104850048-104850049	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs527734727	chr7:104850096-104850097	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371362782	chr7:104850097-104850098	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558248894	chr7:104850167-104850168	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371255267	chr7:104850178-104850179	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs3839740	chr7:104850191-104850192	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547697122	chr7:104850236-104850237	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs147044799	chr7:104850276-104850277	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561548930	chr7:104850280-104850281	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530217692	chr7:104850353-104850354	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200441908	chr7:104850354-104850355	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs111512963	chr7:104850381-104850382	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs538307769	chr7:104850389-104850390	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs79011067	chr7:104850487-104850488	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138271455	chr7:104850514-104850515	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368854994	chr7:104850536-104850537	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs76005462	chr7:104850545-104850546	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551355220	chr7:104850567-104850568	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190231510	chr7:104850568-104850569	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181369409	chr7:104850592-104850593	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144145442	chr7:104850627-104850628	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573812978	chr7:104850652-104850653	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536035662	chr7:104850784-104850785	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146901179	chr7:104850794-104850795	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75301811	chr7:104850860-104850861	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185253371	chr7:104850861-104850862	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190651673	chr7:104850896-104850897	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564909128	chr7:104850898-104850899	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75834379	chr7:104850958-104850959	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541549437	chr7:104850959-104850960	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561206021	chr7:104851006-104851007	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530367627	chr7:104851014-104851015	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569588702	chr7:104851028-104851029	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550206161	chr7:104851033-104851034	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113838378	chr7:104851065-104851066	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565124924	chr7:104851078-104851079	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs571324968	chr7:104851086-104851087	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs182941804	chr7:104851089-104851090	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568415639	chr7:104851090-104851091	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536192311	chr7:104851137-104851138	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs62484665	chr7:104851164-104851165	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571225580	chr7:104851212-104851213	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:8273 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104754400-104850400	Weak transcription	Fetal Kidney	kidney
2	chr7:104822000-104858800	Weak transcription	Gastric	stomach
3	chr7:104827400-104850400	Weak transcription	Aorta	Aorta
4	chr7:104828600-104851000	Weak transcription	Stomach Mucosa	stomach
5	chr7:104828800-104850000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:104830600-104850600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:104831200-104851000	Weak transcription	Pancreas	Pancrea
8	chr7:104833800-104850000	Weak transcription	Fetal Brain Female	brain
9	chr7:104834200-104850000	Weak transcription	Brain Germinal Matrix	brain
10	chr7:104834600-104851000	Weak transcription	Small Intestine	intestine
11	chr7:104838000-104849800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:104838600-104849800	Weak transcription	Fetal Brain Male	brain
13	chr7:104838600-104850400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr7:104839000-104849800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:104839400-104858400	Weak transcription	NHLF	lung
16	chr7:104839600-104850600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:104839600-104857200	Weak transcription	A549	lung
18	chr7:104840000-104850000	Weak transcription	HSMM	muscle
19	chr7:104840600-104849800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr7:104841200-104853400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:104841600-104851200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:104842000-104850400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:104842000-104851000	Weak transcription	Ovary	ovary
24	chr7:104842000-104851000	Weak transcription	HUVEC	blood vessel
25	chr7:104842200-104865400	Weak transcription	K562	blood
26	chr7:104842400-104850000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:104842400-104857200	Weak transcription	HMEC	breast
28	chr7:104842800-104850400	Weak transcription	Fetal Lung	lung
29	chr7:104842800-104851200	Weak transcription	Esophagus	oesophagus
30	chr7:104843200-104863400	Weak transcription	HepG2	liver
31	chr7:104843600-104851200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:104843800-104851000	Weak transcription	Psoas Muscle	Psoas
33	chr7:104843800-104851000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr7:104843800-104851200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:104843800-104851200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:104843800-104851200	Weak transcription	Right Ventricle	heart
37	chr7:104843800-104851200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr7:104843800-104859600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr7:104844000-104849800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:104844000-104850800	Weak transcription	Liver	Liver
41	chr7:104844000-104863200	Weak transcription	Fetal Intestine Large	intestine
42	chr7:104844200-104851000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:104844200-104851000	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:104844200-104869000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:104844200-104869000	Weak transcription	Fetal Intestine Small	intestine
46	chr7:104844200-104869000	Weak transcription	Fetal Muscle Trunk	muscle
47	chr7:104844400-104851200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:104844400-104851200	Weak transcription	Adipose Nuclei	Adipose
49	chr7:104844600-104857800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:104845200-104851800	Enhancers	Primary T helper cells PMA-I stimulated	--

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