Variant report

Variant	nsv427799
Chromosome Location	chr7:103250733-103454202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1459)
CpG islands
(count:306)
Chromatin interactive
region (count:158)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103303101-103303301	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:103301632-103301797	K562	blood:	n/a	n/a
3	ARID3A	chr7:103297830-103298390	K562	blood:	n/a	n/a
4	ARID3A	chr7:103300792-103301326	K562	blood:	n/a	n/a
5	ARID3A	chr7:103331784-103332058	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:103450818-103451255	K562	blood:	n/a	n/a
7	ARID3A	chr7:103450506-103450884	HepG2	liver:	n/a	chr7:103450517-103450533 chr7:103450516-103450532
8	ARID3A	chr7:103272498-103272859	K562	blood:	n/a	n/a
9	ARID3A	chr7:103319899-103320230	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:103300589-103301706	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:103254955-103255128	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:103424189-103424280	K562	blood:	n/a	n/a
13	ARID3A	chr7:103292475-103292581	K562	blood:	n/a	n/a
14	ARID3A	chr7:103298538-103298740	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:103305068-103305251	K562	blood:	n/a	n/a
16	ARID3A	chr7:103345499-103345520	K562	blood:	n/a	n/a
17	ARID3A	chr7:103254691-103255182	K562	blood:	n/a	n/a
18	ATF1	chr7:103297848-103298247	K562	blood:	n/a	n/a
19	ATF1	chr7:103450094-103450336	K562	blood:	n/a	n/a
20	ATF1	chr7:103413091-103413153	K562	blood:	n/a	n/a
21	ATF1	chr7:103393468-103393711	K562	blood:	n/a	n/a
22	ATF1	chr7:103270803-103271170	K562	blood:	n/a	n/a
23	ATF1	chr7:103301009-103301317	K562	blood:	n/a	n/a
24	ATF1	chr7:103272544-103272989	K562	blood:	n/a	n/a
25	ATF1	chr7:103254370-103255262	K562	blood:	n/a	n/a
26	ATF3	chr7:103300900-103301322	K562	blood:	n/a	n/a
27	ATF3	chr7:103297853-103298436	K562	blood:	n/a	n/a
28	ATF3	chr7:103450837-103451209	K562	blood:	n/a	n/a
29	ATF3	chr7:103270774-103271095	K562	blood:	n/a	n/a
30	ATF3	chr7:103254679-103254888	K562	blood:	n/a	n/a
31	BACH1	chr7:103272623-103272854	K562	blood:	n/a	n/a
32	BACH1	chr7:103452349-103452618	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:103423293-103423333	K562	blood:	n/a	n/a
34	BACH1	chr7:103450899-103451214	K562	blood:	n/a	n/a
35	BCLAF1	chr7:103297809-103298425	K562	blood:	n/a	n/a
36	BHLHE40	chr7:103298673-103298683	K562	blood:	n/a	n/a
37	BHLHE40	chr7:103407403-103407486	K562	blood:	n/a	n/a
38	BHLHE40	chr7:103300881-103301800	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:103297004-103297036	K562	blood:	n/a	n/a
40	BHLHE40	chr7:103254146-103254993	K562	blood:	n/a	n/a
41	BHLHE40	chr7:103452421-103452725	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:103297785-103298424	K562	blood:	n/a	n/a
43	BHLHE40	chr7:103298944-103299312	K562	blood:	n/a	n/a
44	BHLHE40	chr7:103300976-103301276	HepG2	liver:	n/a	n/a
45	BHLHE40	chr7:103450748-103451309	K562	blood:	n/a	n/a
46	BHLHE40	chr7:103452606-103452777	K562	blood:	n/a	n/a
47	BHLHE40	chr7:103300942-103301872	K562	blood:	n/a	n/a
48	BRCA1	chr7:103375834-103376215	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:103301680-103301812	GM12878	blood:	n/a	n/a
50	BRCA1	chr7:103358933-103360030	Hela-S3	cervix:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103301932-103301982	HCT-116	colon:	n/a
2	chr7:103301932-103301982	HCT-116	colon:	n/a
3	chr7:103343261-103343311	Jurkat	blood:	n/a
4	chr7:103260062-103260112	GM12878	blood:	n/a
5	chr7:103301932-103301982	CMK	blood:	n/a
6	chr7:103301932-103301982	HRE	kidney:	n/a
7	chr7:103449893-103449943	SK-N-MC	brain:	n/a
8	chr7:103260062-103260112	IMR90	lung:	fetal
9	chr7:103343261-103343311	Caco-2	colon:	n/a
10	chr7:103301932-103301982	HAEpiC	amniotic membrane:	n/a
11	chr7:103449893-103449943	K562	blood:	n/a
12	chr7:103449893-103449943	PANC-1	pancreas:	n/a
13	chr7:103343261-103343311	PFSK-1	brain:	n/a
14	chr7:103449893-103449943	AG04449	skin:	fetal
15	chr7:103279088-103279138	HAEpiC	amniotic membrane:	n/a
16	chr7:103449893-103449943	HCF	heart:	n/a
17	chr7:103260062-103260112	HEEpiC	esophagus:	n/a
18	chr7:103301932-103301982	HIPEpiC	eye:	n/a
19	chr7:103279088-103279138	HCT-116	colon:	n/a
20	chr7:103260062-103260112	HepG2	liver:	n/a
21	chr7:103301932-103301982	AG10803	skin:	n/a
22	chr7:103449893-103449943	ProgFib	skin:	n/a
23	chr7:103279088-103279138	NT2-D1	testis:	n/a
24	chr7:103279088-103279138	HEEpiC	esophagus:	n/a
25	chr7:103301932-103301982	T-47D	breast:	n/a
26	chr7:103449893-103449943	AoSMC	blood vessel:	n/a
27	chr7:103449893-103449943	NB4	blood:	n/a
28	chr7:103449893-103449943	GM19239	blood:	n/a
29	chr7:103449893-103449943	AG04450	lung:	fetal
30	chr7:103279088-103279138	HCF	heart:	n/a
31	chr7:103260062-103260112	HL-60	blood:	n/a
32	chr7:103301932-103301982	GM06990	blood:	n/a
33	chr7:103449893-103449943	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:103449893-103449943	GM12891	blood:	n/a
35	chr7:103449893-103449943	HepG2	liver:	n/a
36	chr7:103343261-103343311	LNCaP	prostate:	n/a
37	chr7:103301932-103301982	AG09319	gingival:	n/a
38	chr7:103260062-103260112	HAEpiC	amniotic membrane:	n/a
39	chr7:103343261-103343311	HMEC	breast:	n/a
40	chr7:103449893-103449943	HCT-116	colon:	n/a
41	chr7:103343261-103343311	SAEC	small airway:	n/a
42	chr7:103260062-103260112	Hepatocyte	liver:	n/a
43	chr7:103279088-103279138	GM06990	blood:	n/a
44	chr7:103279088-103279138	HCM	heart:	n/a
45	chr7:103260062-103260112	HCT-116	colon:	n/a
46	chr7:103260062-103260112	SKMC	muscle:	n/a
47	chr7:103260062-103260112	Jurkat	blood:	n/a
48	chr7:103343261-103343311	T-47D	breast:	n/a
49	chr7:103343261-103343311	NT2-D1	testis:	n/a
50	chr7:103279088-103279138	AG10803	skin:	n/a

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:103290439..103294290-chr7:103295616..103299130,4	K562	blood:
2	chr7:103254507..103256433-chr7:103303415..103304942,2	K562	blood:
3	chr7:103199365..103201003-chr7:103418048..103420205,2	K562	blood:
4	chr7:103304565..103307754-chr7:103310017..103312490,3	MCF-7	breast:
5	chr7:103432622..103435119-chr7:103435202..103437569,2	K562	blood:
6	chr7:103417666..103419702-chr7:103422926..103424579,2	K562	blood:
7	chr7:103262757..103265718-chr7:103587401..103589902,2	K562	blood:
8	chr7:103253081..103256166-chr7:103404446..103406601,3	K562	blood:
9	chr7:103164482..103165037-chr7:103393511..103394116,2	K562	blood:
10	chr7:103299107..103301619-chr7:103313448..103316125,2	K562	blood:
11	chr7:103270998..103273560-chr7:103345066..103347137,2	K562	blood:
12	chr7:103340428..103342815-chr7:103361893..103364250,2	K562	blood:
13	chr7:103438609..103440758-chr7:103446017..103447792,2	K562	blood:
14	chr7:103274516..103276734-chr7:103323210..103324865,2	K562	blood:
15	chr7:103374430..103376979-chr7:103378353..103381015,4	K562	blood:
16	chr7:103253816..103255808-chr7:103257490..103259015,2	K562	blood:
17	chr7:103419863..103421657-chr7:103433485..103435667,2	K562	blood:
18	chr7:103287552..103290222-chr7:103293075..103295780,3	K562	blood:
19	chr7:103414281..103416432-chr7:103424454..103426035,2	K562	blood:
20	chr7:103302444..103304759-chr7:103358804..103361595,2	K562	blood:
21	chr7:103253050..103254714-chr7:103265200..103267338,2	MCF-7	breast:
22	chr7:103404584..103406176-chr7:103410520..103412524,2	K562	blood:
23	chr7:103331525..103333505-chr7:103337273..103339840,2	K562	blood:
24	chr7:103357438..103359358-chr7:103364069..103366186,2	K562	blood:
25	chr7:103265123..103267515-chr7:103269219..103272108,3	K562	blood:
26	chr7:103357438..103359358-chr7:103364069..103366186,2	K562	blood:
27	chr7:103422935..103424556-chr7:103443024..103444916,2	K562	blood:
28	chr7:103334750..103336512-chr7:103338855..103341152,3	K562	blood:
29	chr7:103442619..103446141-chr7:103451934..103454148,3	K562	blood:
30	chr7:103432622..103435119-chr7:103435202..103437569,2	K562	blood:
31	chr7:103296674..103299385-chr7:103636597..103638114,2	K562	blood:
32	chr7:103335628..103338296-chr7:103339379..103341676,2	K562	blood:
33	chr7:103452464..103456150-chr7:103461161..103465020,4	K562	blood:
34	chr7:103287552..103290222-chr7:103293075..103295780,3	K562	blood:
35	chr7:103354410..103357861-chr7:103367523..103371715,4	K562	blood:
36	chr7:103297074..103301566-chr7:103303216..103306956,8	K562	blood:
37	chr7:103423396..103425978-chr7:103435870..103438560,2	K562	blood:
38	chr7:103253287..103254849-chr7:103287404..103290090,2	K562	blood:
39	chr7:103374430..103376979-chr7:103378353..103381015,4	K562	blood:
40	chr7:103297764..103300699-chr7:103309943..103311774,3	K562	blood:
41	chr7:103302157..103305081-chr7:103307428..103309222,2	K562	blood:
42	chr7:103304565..103307754-chr7:103310017..103312490,3	MCF-7	breast:
43	chr7:103270998..103273560-chr7:103345066..103347137,2	K562	blood:
44	chr7:103403884..103405527-chr7:103424652..103427237,2	K562	blood:
45	chr7:103313058..103315600-chr7:103766420..103769012,2	K562	blood:
46	chr7:103409588..103414279-chr7:103419372..103424003,5	K562	blood:
47	chr7:103354410..103357861-chr7:103367523..103371715,4	K562	blood:
48	chr7:103254361..103256762-chr7:103277435..103279324,2	K562	blood:
49	chr17:48784748..48785382-chr7:103297553..103298427,2	MCF-7	breast:
50	chr7:103422935..103424556-chr7:103443024..103444916,2	K562	blood:

No data

Variant related genes	Relation type
RELN	TF binding region
RELN	CpG island
ENSG00000189056	chromatin interactions
ENSG00000154945	chromatin interactions

Extended variants
information (count: 8602 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:8602 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76328156	chr7:103250747-103250748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180928940	chr7:103250757-103250758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564027008	chr7:103250765-103250766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551858658	chr7:103250766-103250767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35205780	chr7:103250816-103250817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531537196	chr7:103250845-103250846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376858803	chr7:103250846-103250847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534373998	chr7:103250848-103250849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144505756	chr7:103250852-103250853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565981478	chr7:103250860-103250861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543583937	chr7:103250868-103250869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555278907	chr7:103250912-103250913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576628427	chr7:103250987-103250988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113762825	chr7:103250994-103250995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113624447	chr7:103251041-103251042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561706931	chr7:103251062-103251063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374595649	chr7:103251071-103251072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370146263	chr7:103251112-103251113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147994579	chr7:103251116-103251117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186983114	chr7:103251131-103251132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370615329	chr7:103251133-103251134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201003473	chr7:103251158-103251159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs362691	chr7:103251161-103251162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138598422	chr7:103251196-103251197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143972828	chr7:103251206-103251207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373969392	chr7:103251212-103251213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3025962	chr7:103251218-103251219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs544486809	chr7:103251234-103251235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3025963	chr7:103251253-103251254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555808266	chr7:103251289-103251290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377571746	chr7:103251303-103251304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34465360	chr7:103251305-103251306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35566699	chr7:103251320-103251321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541626088	chr7:103251340-103251341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563622992	chr7:103251348-103251349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs362692	chr7:103251383-103251384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552159783	chr7:103251403-103251404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563780565	chr7:103251409-103251410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141635276	chr7:103251427-103251428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192292043	chr7:103251449-103251450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567801089	chr7:103251520-103251521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536467086	chr7:103251550-103251551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548354839	chr7:103251583-103251584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372861981	chr7:103251596-103251597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548468563	chr7:103251608-103251609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73714478	chr7:103251635-103251636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs537308240	chr7:103251663-103251664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566975040	chr7:103251668-103251669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183433702	chr7:103251781-103251782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145952336	chr7:103251799-103251800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Gastric cancer	24379144	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
Prostate cancer	16461572	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
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103245000-103251800	Weak transcription	K562	blood
2	chr7:103245000-103259600	Weak transcription	HepG2	liver
3	chr7:103251800-103252200	Strong transcription	K562	blood
4	chr7:103252200-103254000	Weak transcription	K562	blood
5	chr7:103253600-103255400	Enhancers	Fetal Heart	heart
6	chr7:103254000-103254400	Enhancers	Left Ventricle	heart
7	chr7:103254000-103255000	Enhancers	K562	blood
8	chr7:103254800-103255200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:103255000-103255400	Flanking Active TSS	K562	blood
10	chr7:103255200-103255400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:103255400-103256200	Enhancers	K562	blood
12	chr7:103255800-103256800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:103256000-103256800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:103256200-103269000	Weak transcription	K562	blood
15	chr7:103256800-103265600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:103259600-103260200	Strong transcription	HepG2	liver
17	chr7:103260200-103260400	Enhancers	Stomach Smooth Muscle	stomach
18	chr7:103260200-103267000	Weak transcription	HepG2	liver
19	chr7:103265600-103268400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:103266400-103266600	Enhancers	NHLF	lung
21	chr7:103266600-103270800	Weak transcription	NHLF	lung
22	chr7:103266800-103267200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:103267000-103267600	Strong transcription	HepG2	liver
24	chr7:103267000-103268000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:103267000-103268400	Enhancers	NHDF-Ad	bronchial
26	chr7:103267200-103270800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:103267400-103268000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:103267600-103270000	Weak transcription	HepG2	liver
29	chr7:103268000-103270600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:103268000-103272600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:103268400-103270800	Weak transcription	NHDF-Ad	bronchial
32	chr7:103268400-103273600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:103269000-103270800	Strong transcription	K562	blood
34	chr7:103270000-103271200	Strong transcription	HepG2	liver
35	chr7:103270600-103271000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:103270600-103271200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr7:103270800-103271000	Enhancers	HUVEC	blood vessel
38	chr7:103270800-103271000	Enhancers	NHEK	skin
39	chr7:103270800-103271200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:103270800-103271200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:103270800-103271200	Enhancers	NH-A	brain
42	chr7:103270800-103271200	Enhancers	NHDF-Ad	bronchial
43	chr7:103270800-103271200	Enhancers	NHLF	lung
44	chr7:103270800-103271400	Genic enhancers	K562	blood
45	chr7:103271000-103271200	Enhancers	HMEC	breast
46	chr7:103271000-103272600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:103271200-103272400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr7:103271200-103272600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:103271200-103272600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:103271200-103272600	Weak transcription	NH-A	brain

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