Variant report

Variant	nsv1029832
Chromosome Location	chr7:104905057-105112489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3213)
CpG islands
(count:1709)
Chromatin interactive
region (count:202)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3213 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
2	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
3	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
4	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
6	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
7	ARID3A	chr7:104924529-104924792	K562	blood:	n/a	n/a
8	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
10	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
11	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
12	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
13	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
18	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
19	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
20	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
22	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
24	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
25	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
26	ARID3A	chr7:104909404-104910342	K562	blood:	n/a	chr7:104910069-104910085 chr7:104909863-104909879 chr7:104909862-104909878
27	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
28	ARID3A	chr7:104909503-104909771	HepG2	liver:	n/a	n/a
29	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
30	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
31	ATF1	chr7:104908668-104908848	K562	blood:	n/a	n/a
32	ATF2	chr7:104992448-104993159	GM12878	blood:	n/a	n/a
33	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a
34	ATF3	chr7:104944489-104944823	HCT-116	colon:	n/a	n/a
35	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
37	BACH1	chr7:104952147-104952403	K562	blood:	n/a	n/a
38	BACH1	chr7:105029716-105030051	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr7:104922679-104922809	K562	blood:	n/a	n/a
41	BACH1	chr7:104949880-104950067	K562	blood:	n/a	n/a
42	BACH1	chr7:105042903-105043365	K562	blood:	n/a	n/a
43	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a
44	BATF	chr7:105084864-105085128	GM12878	blood:	n/a	n/a
45	BATF	chr7:104992598-104992866	GM12878	blood:	n/a	n/a
46	BATF	chr7:104920106-104920379	GM12878	blood:	n/a	n/a
47	BATF	chr7:105041762-105041974	GM12878	blood:	n/a	n/a
48	BATF	chr7:104944451-104945258	GM12878	blood:	n/a	chr7:104945126-104945136
49	BATF	chr7:104919833-104920062	GM12878	blood:	n/a	chr7:104919902-104919913
50	BATF	chr7:104908573-104908798	GM12878	blood:	n/a	chr7:104908640-104908651

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105018109-105018159	ovcar-3	ovarian:	n/a
2	chr7:105018109-105018159	ovcar-3	ovarian:	n/a
3	chr7:104943515-104943565	SK-N-MC	brain:	n/a
4	chr7:105029492-105029542	ECC-1	luminal epithelium:	n/a
5	chr7:105110948-105110998	U87	brain:	n/a
6	chr7:105029895-105029945	HRCEpiC	kidney:	n/a
7	chr7:105029499-105029549	HCM	heart:	n/a
8	chr7:105079663-105079713	ProgFib	skin:	n/a
9	chr7:105028539-105028589	HIPEpiC	eye:	n/a
10	chr7:105029125-105029175	AG04449	skin:	fetal
11	chr7:105030168-105030218	LNCaP	prostate:	n/a
12	chr7:104939331-104939381	AG09319	gingival:	n/a
13	chr7:105018109-105018159	NH-A	brain:	n/a
14	chr7:105079663-105079713	HCPEpiC	choroid plexus:	n/a
15	chr7:105027541-105027591	HEK293	kidney:	embryo
16	chr7:105029385-105029435	U87	brain:	n/a
17	chr7:105026171-105026221	ovcar-3	ovarian:	n/a
18	chr7:104941977-104942027	Jurkat	blood:	n/a
19	chr7:104941898-104941948	GM19239	blood:	n/a
20	chr7:105026171-105026221	HRCEpiC	kidney:	n/a
21	chr7:105029497-105029547	AG10803	skin:	n/a
22	chr7:104941898-104941948	H1-hESC	embryonic stem cell:	embryo
23	chr7:104941821-104941871	HCM	heart:	n/a
24	chr7:104981497-104981547	SK-N-SH	brain:	n/a
25	chr7:104945248-104945298	AoSMC	blood vessel:	n/a
26	chr7:105110948-105110998	HCF	heart:	n/a
27	chr7:105094993-105095043	HUVEC	blood vessel:	n/a
28	chr7:105030752-105030802	SKMC	muscle:	n/a
29	chr7:105029485-105029535	BE2_C	brain:	n/a
30	chr7:104939331-104939381	U87	brain:	n/a
31	chr7:105097168-105097218	GM12892	blood:	n/a
32	chr7:104909815-104909865	LNCaP	prostate:	n/a
33	chr7:105028539-105028589	MCF10A-Er-Src	breast:	n/a
34	chr7:105029125-105029175	AG09319	gingival:	n/a
35	chr7:104909815-104909865	K562	blood:	n/a
36	chr7:104939331-104939381	T-47D	breast:	n/a
37	chr7:104941898-104941948	HAEpiC	amniotic membrane:	n/a
38	chr7:105026171-105026221	SK-N-SH	brain:	n/a
39	chr7:104945248-104945298	ovcar-3	ovarian:	n/a
40	chr7:105097168-105097218	HL-60	blood:	n/a
41	chr7:104941821-104941871	HRPEpiC	eye:	n/a
42	chr7:105029895-105029945	NB4	blood:	n/a
43	chr7:104943515-104943565	Hepatocyte	liver:	n/a
44	chr7:105026171-105026221	BE2_C	brain:	n/a
45	chr7:105029385-105029435	GM06990	blood:	n/a
46	chr7:105029492-105029542	HNPCEpiC	eye:	n/a
47	chr7:105097168-105097218	H1-hESC	embryonic stem cell:	embryo
48	chr7:105029895-105029945	BE2_C	brain:	n/a
49	chr7:105079663-105079713	HEEpiC	esophagus:	n/a
50	chr7:105029499-105029549	PFSK-1	brain:	n/a

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:105016302..105018652-chr7:105027482..105029964,4	K562	blood:
2	chr7:104922381..104923956-chr7:104935072..104936834,2	MCF-7	breast:
3	chr7:104924058..104925116-chr7:104956648..104957763,18	MCF-7	breast:
4	chr7:105012234..105014245-chr7:105022510..105026066,3	K562	blood:
5	chr7:104984088..104985686-chr7:105028114..105030701,2	MCF-7	breast:
6	chr7:105077610..105079593-chr7:105277215..105278771,2	MCF-7	breast:
7	chr7:104965775..104968018-chr7:104970482..104972338,2	MCF-7	breast:
8	chr7:104944150..104946367-chr7:104948630..104950865,4	MCF-7	breast:
9	chr7:105024723..105026503-chr7:105037837..105040106,2	K562	blood:
10	chr7:104924058..104925048-chr7:104956656..104957758,5	MCF-7	breast:
11	chr7:104935439..104938791-chr7:104944886..104947910,3	MCF-7	breast:
12	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
13	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
14	chr7:104793089..104794036-chr7:104976109..104977046,2	MCF-7	breast:
15	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:
16	chr7:104985604..104988009-chr7:104988661..104992551,3	MCF-7	breast:
17	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
18	chr7:105009408..105012962-chr7:105018316..105021525,4	K562	blood:
19	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
20	chr7:104651368..104653205-chr7:105026206..105027848,2	K562	blood:
21	chr7:104651667..104654788-chr7:105068823..105071945,3	MCF-7	breast:
22	chr7:104914487..104916145-chr7:104922195..104924067,2	K562	blood:
23	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
24	chr7:104955875..104958627-chr7:104961394..104962913,2	MCF-7	breast:
25	chr7:105026975..105030937-chr7:105032940..105036440,7	K562	blood:
26	chr7:104960628..104963813-chr7:104964024..104966847,3	MCF-7	breast:
27	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
28	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
29	chr7:104981388..104983616-chr7:105078711..105081522,2	MCF-7	breast:
30	chr7:104970519..104973414-chr7:104974940..104976942,3	MCF-7	breast:
31	chr7:105069185..105071026-chr7:105110310..105112272,2	MCF-7	breast:
32	chr7:104944468..104948806-chr7:104949907..104951559,3	K562	blood:
33	chr7:105088778..105090320-chr7:105090980..105093442,3	MCF-7	breast:
34	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
35	chr7:105041786..105042328-chr7:105128303..105129103,3	MCF-7	breast:
36	chr7:104956925..104959493-chr7:105027224..105029889,3	MCF-7	breast:
37	chr7:104957510..104959385-chr7:104965005..104966675,2	MCF-7	breast:
38	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
39	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
40	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
41	chr7:104945324..104947368-chr7:104952699..104954590,2	K562	blood:
42	chr7:105039077..105041810-chr7:105045428..105047601,2	K562	blood:
43	chr7:104907817..104909444-chr7:104949572..104952100,2	MCF-7	breast:
44	chr7:104905870..104907501-chr7:104908223..104910531,2	K562	blood:
45	chr7:105038088..105039818-chr7:105043302..105044828,3	K562	blood:
46	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
47	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
48	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
49	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
50	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
2	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
3	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614
4	lnc-SRPK2-5	chr7:104909253-104909316	NONHSAT122614
5	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
6	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1

No data

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

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

Variant related genes	Relation type
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
RWDD4P1	CpG island
RNU6-1322P	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000080298	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000244490	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000160999	chromatin interactions

Extended variants
information (count: 8107 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:8107 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12668040	chr7:104905057-104905058	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572615200	chr7:104905083-104905084	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527979556	chr7:104905100-104905101	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141350309	chr7:104905102-104905103	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566358361	chr7:104905116-104905117	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535401569	chr7:104905145-104905146	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs76925721	chr7:104905186-104905187	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187996639	chr7:104905230-104905231	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2299327	chr7:104905252-104905253	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537536339	chr7:104905263-104905264	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs6945585	chr7:104905277-104905278	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571382585	chr7:104905412-104905413	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533861802	chr7:104905421-104905422	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549874538	chr7:104905468-104905469	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554008766	chr7:104905491-104905492	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150237045	chr7:104905499-104905500	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543078598	chr7:104905519-104905520	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544638007	chr7:104905554-104905555	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2299328	chr7:104905588-104905589	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs144960434	chr7:104905605-104905606	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2299329	chr7:104905613-104905614	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572925083	chr7:104905736-104905737	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs180860129	chr7:104905749-104905750	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530428089	chr7:104905751-104905752	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185577454	chr7:104905759-104905760	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs7783860	chr7:104905782-104905783	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547594224	chr7:104905783-104905784	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561651851	chr7:104905797-104905798	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530310533	chr7:104905818-104905819	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548608374	chr7:104905836-104905837	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138651468	chr7:104905852-104905853	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531316502	chr7:104905869-104905870	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376262265	chr7:104905887-104905888	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551029250	chr7:104905904-104905905	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571377625	chr7:104905980-104905981	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534022261	chr7:104905994-104905995	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115793282	chr7:104906054-104906055	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2299330	chr7:104906070-104906071	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536549297	chr7:104906078-104906079	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540902065	chr7:104906081-104906082	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557221075	chr7:104906087-104906088	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556601429	chr7:104906237-104906238	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142944760	chr7:104906276-104906277	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545532038	chr7:104906288-104906289	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34042895	chr7:104906308-104906309	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397826925	chr7:104906316-104906317	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs79502336	chr7:104906317-104906318	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186890809	chr7:104906367-104906368	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369398118	chr7:104906370-104906371	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138170429	chr7:104906395-104906396	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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

Chromatin state (count:4094 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104869600-104909200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:104879000-104907800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:104885400-104907000	Weak transcription	Fetal Intestine Small	intestine
4	chr7:104886400-104916600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:104891600-104907800	Weak transcription	Aorta	Aorta
6	chr7:104892200-104906600	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:104896400-104909000	Weak transcription	Pancreas	Pancrea
8	chr7:104897000-104905400	Weak transcription	Fetal Brain Male	brain
9	chr7:104897600-104906800	Weak transcription	Right Ventricle	heart
10	chr7:104897600-104907400	Weak transcription	Right Atrium	heart
11	chr7:104898000-104907200	Weak transcription	Fetal Kidney	kidney
12	chr7:104898200-104907200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:104898600-104905800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr7:104898600-104909000	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr7:104898600-104909000	Weak transcription	Small Intestine	intestine
16	chr7:104898800-104906000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr7:104898800-104906400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr7:104898800-104907800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr7:104898800-104907800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:104899000-104905800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:104899000-104906800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:104899400-104907000	Weak transcription	Primary B cells from cord blood	blood
23	chr7:104901800-104905400	Enhancers	Fetal Thymus	thymus
24	chr7:104902200-104905800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr7:104902200-104906400	Transcr. at gene 5' and 3'	Dnd41	blood
26	chr7:104902400-104906800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:104902600-104905200	Weak transcription	Ovary	ovary
28	chr7:104902600-104905400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:104902600-104905800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:104902600-104906400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:104902600-104907000	Weak transcription	Adipose Nuclei	Adipose
32	chr7:104902600-104907000	Weak transcription	HSMM	muscle
33	chr7:104902600-104907200	Weak transcription	Fetal Heart	heart
34	chr7:104902600-104907200	Weak transcription	NHLF	lung
35	chr7:104902600-104907400	Weak transcription	Hela-S3	cervix
36	chr7:104902600-104907600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:104902600-104907600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:104902600-104907600	Weak transcription	NHDF-Ad	bronchial
39	chr7:104902600-104907800	Weak transcription	Liver	Liver
40	chr7:104902600-104907800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr7:104902600-104907800	Weak transcription	Osteobl	bone
42	chr7:104902600-104908000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr7:104902800-104905600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr7:104902800-104907200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:104902800-104907200	Weak transcription	HSMMtube	muscle
46	chr7:104902800-104908400	Weak transcription	A549	lung
47	chr7:104903000-104905400	Weak transcription	NHEK	skin
48	chr7:104903000-104906800	Weak transcription	Primary T cells from cord blood	blood
49	chr7:104903000-104907000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr7:104903000-104907200	Weak transcription	Fetal Brain Female	brain

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