Variant report

Variant	esv2758127
Chromosome Location	chr7:104766707-105110581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4658)
CpG islands
(count:2873)
Chromatin interactive
region (count:356)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4658 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104819987-104820013	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:104873284-104873810	K562	blood:	n/a	n/a
3	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
4	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
5	ARID3A	chr7:104897645-104898076	K562	blood:	n/a	n/a
6	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
7	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
8	ARID3A	chr7:104909404-104910342	K562	blood:	n/a	chr7:104910069-104910085 chr7:104909863-104909879 chr7:104909862-104909878
9	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
12	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
14	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
15	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
16	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
17	ARID3A	chr7:104819345-104819786	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
19	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
20	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
22	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
24	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
25	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
26	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
27	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
28	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
29	ARID3A	chr7:104924529-104924792	K562	blood:	n/a	n/a
30	ARID3A	chr7:104771489-104772167	K562	blood:	n/a	n/a
31	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
32	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
33	ARID3A	chr7:104909503-104909771	HepG2	liver:	n/a	n/a
34	ATF1	chr7:104908668-104908848	K562	blood:	n/a	n/a
35	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
36	ATF1	chr7:104897712-104898056	K562	blood:	n/a	n/a
37	ATF1	chr7:104902188-104902552	K562	blood:	n/a	n/a
38	ATF1	chr7:104897219-104897309	K562	blood:	n/a	n/a
39	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
40	ATF1	chr7:104771466-104772161	K562	blood:	n/a	n/a
41	ATF1	chr7:104865550-104866001	K562	blood:	n/a	n/a
42	ATF1	chr7:104796207-104796341	K562	blood:	n/a	n/a
43	ATF2	chr7:104992448-104993159	GM12878	blood:	n/a	n/a
44	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a
45	ATF3	chr7:104944489-104944823	HCT-116	colon:	n/a	n/a
46	BACH1	chr7:104817804-104817817	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr7:104871499-104871667	K562	blood:	n/a	n/a
48	BACH1	chr7:104949880-104950067	K562	blood:	n/a	n/a
49	BACH1	chr7:104771371-104772434	K562	blood:	n/a	n/a
50	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2873 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105029497-105029547	HCF	heart:	n/a
2	chr7:104879299-104879349	PrEC	prostate:	n/a
3	chr7:104772345-104772395	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:105097168-105097218	MCF10A-Er-Src	breast:	n/a
5	chr7:105029499-105029549	HAEpiC	amniotic membrane:	n/a
6	chr7:104776501-104776551	NT2-D1	testis:	n/a
7	chr7:105029497-105029547	HCF	heart:	n/a
8	chr7:104879299-104879349	PrEC	prostate:	n/a
9	chr7:104772345-104772395	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:105097168-105097218	MCF10A-Er-Src	breast:	n/a
11	chr7:105029499-105029549	HAEpiC	amniotic membrane:	n/a
12	chr7:104776501-104776551	NT2-D1	testis:	n/a
13	chr7:104981497-104981547	BE2_C	brain:	n/a
14	chr7:105094993-105095043	HIPEpiC	eye:	n/a
15	chr7:105029497-105029547	HMEC	breast:	n/a
16	chr7:105029895-105029945	SK-N-SH	brain:	n/a
17	chr7:104883450-104883500	HCPEpiC	choroid plexus:	n/a
18	chr7:105030752-105030802	H1-hESC	embryonic stem cell:	embryo
19	chr7:105029497-105029547	NH-A	brain:	n/a
20	chr7:105097168-105097218	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:105029492-105029542	AG09319	gingival:	n/a
22	chr7:104885248-104885298	Caco-2	colon:	n/a
23	chr7:104941977-104942027	HUVEC	blood vessel:	n/a
24	chr7:105028539-105028589	NB4	blood:	n/a
25	chr7:104772345-104772395	HAEpiC	amniotic membrane:	n/a
26	chr7:104892331-104892381	BE2_C	brain:	n/a
27	chr7:105018109-105018159	NHBE	bronchial:	n/a
28	chr7:105094993-105095043	AG09309	skin:	n/a
29	chr7:105028539-105028589	ECC-1	luminal epithelium:	n/a
30	chr7:104869288-104869338	A549	lung:	n/a
31	chr7:104892331-104892381	HUVEC	blood vessel:	n/a
32	chr7:104888858-104888908	SK-N-MC	brain:	n/a
33	chr7:104941977-104942027	Caco-2	colon:	n/a
34	chr7:104869189-104869239	MCF10A-Er-Src	breast:	n/a
35	chr7:104909815-104909865	HRE	kidney:	n/a
36	chr7:104994322-104994372	NHDF-neo	bronchial:	n/a
37	chr7:104776501-104776551	K562	blood:	n/a
38	chr7:105018109-105018159	HIPEpiC	eye:	n/a
39	chr7:105097168-105097218	HEEpiC	esophagus:	n/a
40	chr7:105029492-105029542	GM06990	blood:	n/a
41	chr7:104892331-104892381	PANC-1	pancreas:	n/a
42	chr7:104945248-104945298	HRCEpiC	kidney:	n/a
43	chr7:104892331-104892381	SAEC	small airway:	n/a
44	chr7:105079663-105079713	NHDF-neo	bronchial:	n/a
45	chr7:104885108-104885158	AG10803	skin:	n/a
46	chr7:105029485-105029535	GM12892	blood:	n/a
47	chr7:104887042-104887092	U87	brain:	n/a
48	chr7:104909430-104909480	AG09319	gingival:	n/a
49	chr7:105079663-105079713	HEEpiC	esophagus:	n/a
50	chr7:104837830-104837880	NH-A	brain:	n/a

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
2	chr7:104772764..104774362-chr7:104793960..104796618,2	K562	blood:
3	chr7:105029252..105029910-chr9:3525726..3526715,2	NB4	blood:
4	chr7:104767690..104770520-chr7:104772905..104776703,4	MCF-7	breast:
5	chr7:104649613..104651128-chr7:104876520..104878391,2	K562	blood:
6	chr7:104873668..104875334-chr7:104875685..104877257,2	MCF-7	breast:
7	chr7:104932192..104934225-chr7:104942946..104944763,2	MCF-7	breast:
8	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
9	chr7:104620361..104623335-chr7:104771207..104773173,3	K562	blood:
10	chr7:104834936..104837712-chr7:104838774..104840413,2	MCF-7	breast:
11	chr7:104914487..104916145-chr7:104922195..104924067,2	K562	blood:
12	chr7:104996114..104998066-chr7:105006500..105008822,2	K562	blood:
13	chr7:104653211..104654776-chr7:105027099..105029228,2	K562	blood:
14	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
15	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
16	chr7:104994593..104996936-chr7:105006253..105008097,2	K562	blood:
17	chr7:104778242..104779954-chr7:105027433..105030431,2	MCF-7	breast:
18	chr7:105039769..105040575-chr7:105229933..105230493,2	MCF-7	breast:
19	chr7:104935027..104937759-chr7:104947845..104950749,2	K562	blood:
20	chr7:104906464..104909306-chr7:104939170..104942038,3	MCF-7	breast:
21	chr7:104653252..104654991-chr7:104961759..104964369,2	MCF-7	breast:
22	chr7:104994593..104996936-chr7:105006253..105008097,2	K562	blood:
23	chr7:104890216..104893018-chr7:104897423..104900351,2	K562	blood:
24	chr7:104791198..104793331-chr7:104802903..104805814,2	K562	blood:
25	chr7:104943318..104946165-chr7:104949324..104952244,3	K562	blood:
26	chr7:104890079..104892213-chr7:104894291..104897029,3	K562	blood:
27	chr7:104890079..104892213-chr7:104894291..104897029,3	K562	blood:
28	chr7:104855097..104857884-chr7:104863691..104866292,2	K562	blood:
29	chr7:104652893..104655901-chr7:105027705..105031319,8	MCF-7	breast:
30	chr7:105038088..105039818-chr7:105043302..105044810,2	K562	blood:
31	chr7:104652804..104654779-chr7:104780043..104781803,2	MCF-7	breast:
32	chr7:105078529..105081334-chr7:105089630..105092260,2	MCF-7	breast:
33	chr7:104924058..104925116-chr7:104956648..104957763,18	MCF-7	breast:
34	chr7:105041648..105042543-chr7:105069609..105070839,7	MCF-7	breast:
35	chr7:104924058..104925048-chr7:104956656..104957758,5	MCF-7	breast:
36	chr7:105028909..105031014-chr7:105085186..105086946,2	K562	blood:
37	chr7:105028707..105032086-chr7:105067490..105070575,3	K562	blood:
38	chr7:104760924..104763369-chr7:104766253..104769218,2	MCF-7	breast:
39	chr16:74733435..74734081-chr7:104874019..104874519,2	Hela-S3	cervix:
40	chr7:104824422..104827358-chr7:104839079..104842407,3	K562	blood:
41	chr7:104893974..104896006-chr7:104900694..104903454,2	K562	blood:
42	chr7:105009330..105013041-chr7:105014599..105017566,3	K562	blood:
43	chr7:105009408..105012962-chr7:105018316..105021525,4	K562	blood:
44	chr7:104851087..104853973-chr7:104856176..104858967,3	K562	blood:
45	chr7:104755331..104758126-chr7:104769285..104772324,4	K562	blood:
46	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
47	chr7:104966725..104970068-chr7:104975373..104978585,3	MCF-7	breast:
48	chr7:104985604..104988009-chr7:104988661..104992551,3	MCF-7	breast:
49	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
50	chr7:104855613..104857301-chr7:104859223..104860789,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MLL5-4	chr7:104829637-104829934	NONHSAT122612
2	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
3	lnc-MLL5-5	chr7:104845047-104845306	NONHSAT122615
4	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
5	lnc-MLL5-4	chr7:104830195-104830261	NONHSAT122612
6	lnc-SRPK2-5	chr7:104844170-104844232	NONHSAT122614
7	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614
8	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
9	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1
10	lnc-SRPK2-5	chr7:104909253-104909316	NONHSAT122614

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
ENSG00000271482	TF binding region
ENSG00000213361	TF binding region
ENSG00000270764	TF binding region
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
ENSG00000271482	CpG island
ENSG00000213361	CpG island
ENSG00000270764	CpG island
RWDD4P1	CpG island
RNU6-1322P	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000005483	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000271482	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000270764	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000244490	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000213361	chromatin interactions

Extended variants
information (count: 13330 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:13330 , 50 per page) page: 1 2 3 4 5 6 7 ... 267

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375304054	chr7:104766715-104766716	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544378514	chr7:104766716-104766717	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1050421	chr7:104766726-104766727	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs1050419	chr7:104766732-104766733	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs1050418	chr7:104766734-104766735	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1050417	chr7:104766738-104766739	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1050416	chr7:104766739-104766740	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs1050415	chr7:104766741-104766742	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs1050413	chr7:104766754-104766755	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1050412	chr7:104766756-104766757	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs1050411	chr7:104766759-104766760	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs141649827	chr7:104766770-104766771	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369044666	chr7:104766785-104766786	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs1131143	chr7:104766786-104766787	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141040841	chr7:104766814-104766815	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200737312	chr7:104766825-104766826	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs182047476	chr7:104766838-104766839	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144222983	chr7:104766858-104766859	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs566770938	chr7:104766927-104766928	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs113563467	chr7:104766991-104766992	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565167899	chr7:104766992-104766993	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529353393	chr7:104767085-104767086	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549259720	chr7:104767140-104767141	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76649164	chr7:104767155-104767156	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531846970	chr7:104767159-104767160	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556101840	chr7:104767161-104767162	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551930504	chr7:104767168-104767169	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571992032	chr7:104767213-104767214	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527955063	chr7:104767236-104767237	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546621716	chr7:104767238-104767239	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566519938	chr7:104767241-104767242	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs114930756	chr7:104767265-104767266	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555204781	chr7:104767279-104767280	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs568911408	chr7:104767281-104767282	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs3815256	chr7:104767295-104767296	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs557897061	chr7:104767315-104767316	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs377118158	chr7:104767317-104767318	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs147938666	chr7:104767330-104767331	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376105085	chr7:104767388-104767389	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs199707529	chr7:104767411-104767412	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553650828	chr7:104767412-104767413	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185114770	chr7:104767429-104767430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs140063535	chr7:104767441-104767442	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs199524118	chr7:104767492-104767493	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370227011	chr7:104767525-104767526	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149705704	chr7:104767526-104767527	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531805240	chr7:104767552-104767553	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201820252	chr7:104767558-104767559	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200765936	chr7:104767588-104767589	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565439252	chr7:104767593-104767594	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Myxofibrosarcoma	20639860	CNVD
Chordoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:8107 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104678000-104812200	Strong transcription	Dnd41	blood
2	chr7:104740400-104787400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:104750200-104777000	Weak transcription	Right Atrium	heart
4	chr7:104752800-104807400	Weak transcription	Fetal Brain Male	brain
5	chr7:104753600-104768000	Weak transcription	Psoas Muscle	Psoas
6	chr7:104753800-104768400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:104753800-104772200	Weak transcription	Aorta	Aorta
8	chr7:104753800-104772800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:104753800-104776600	Weak transcription	Stomach Mucosa	stomach
10	chr7:104753800-104822000	Weak transcription	Small Intestine	intestine
11	chr7:104754400-104776800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:104754400-104850400	Weak transcription	Fetal Kidney	kidney
13	chr7:104755000-104772600	Weak transcription	Fetal Brain Female	brain
14	chr7:104755200-104767000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr7:104755200-104782000	Weak transcription	Colonic Mucosa	Colon
16	chr7:104755600-104776600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr7:104755600-104778200	Weak transcription	Hela-S3	cervix
18	chr7:104755600-104790400	Weak transcription	NH-A	brain
19	chr7:104756400-104779400	Weak transcription	A549	lung
20	chr7:104756400-104806600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:104759800-104769200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:104759800-104788600	Strong transcription	Primary B cells from cord blood	blood
23	chr7:104760000-104773200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr7:104760200-104767200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:104760200-104769800	Weak transcription	HSMMtube	muscle
26	chr7:104760200-104771800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr7:104760200-104772400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:104760400-104776600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:104760400-104781800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:104760800-104781600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr7:104761000-104804600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr7:104761200-104787200	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr7:104761800-104769200	Strong transcription	Primary B cells from peripheral blood	blood
34	chr7:104762000-104766800	Strong transcription	Thymus	Thymus
35	chr7:104762000-104768800	Strong transcription	NHEK	skin
36	chr7:104762200-104766800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:104762400-104787200	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr7:104762600-104771000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:104762800-104768800	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr7:104762800-104785000	Strong transcription	Primary T cells from cord blood	blood
41	chr7:104763000-104767400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:104763000-104769000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr7:104763000-104771400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:104763200-104771800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr7:104763200-104785000	Strong transcription	Fetal Intestine Large	intestine
46	chr7:104763400-104787000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:104763600-104766800	Strong transcription	Fetal Thymus	thymus
48	chr7:104763600-104766800	Strong transcription	Osteobl	bone
49	chr7:104763600-104767400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:104763800-104767200	Strong transcription	Adipose Nuclei	Adipose

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