Variant report

Variant	esv33257
Chromosome Location	chr7:125571419-125743350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:125606321-125606646	GM12878	blood:	n/a	n/a
2	BATF	chr7:125656888-125657086	GM12878	blood:	n/a	chr7:125657018-125657029 chr7:125657002-125657013
3	BHLHE40	chr7:125720305-125720422	GM12878	blood:	n/a	n/a
4	BRCA1	chr7:125661964-125662015	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr7:125574517-125575153	HCT-116	colon:	n/a	n/a
6	CBX3	chr7:125574542-125575099	HCT-116	colon:	n/a	n/a
7	CEBPB	chr7:125628636-125628960	HepG2	liver:	n/a	chr7:125628800-125628811 chr7:125628802-125628811
8	CEBPB	chr7:125719721-125720047	H1-hESC	embryonic stem cell:	n/a	chr7:125719898-125719909 chr7:125719900-125719911 chr7:125719898-125719911
9	CEBPB	chr7:125719752-125720054	IMR90	lung:	n/a	chr7:125719898-125719909 chr7:125719900-125719911 chr7:125719898-125719911
10	CEBPB	chr7:125586220-125586477	A549	lung:	n/a	chr7:125586287-125586298 chr7:125586287-125586296
11	CEBPB	chr7:125628748-125628924	A549	lung:	n/a	chr7:125628800-125628811 chr7:125628802-125628811
12	CEBPB	chr7:125577494-125577627	HepG2	liver:	n/a	chr7:125577588-125577599 chr7:125577589-125577598 chr7:125577589-125577598 chr7:125577587-125577600 chr7:125577587-125577600 chr7:125577589-125577598 chr7:125577587-125577598 chr7:125577589-125577598
13	CEBPB	chr7:125608121-125608318	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:125654878-125655143	Hela-S3	cervix:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
15	CEBPB	chr7:125654844-125655083	H1-hESC	embryonic stem cell:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
16	CEBPB	chr7:125731963-125732282	K562	blood:	n/a	chr7:125732111-125732124 chr7:125732113-125732122 chr7:125732113-125732122 chr7:125732111-125732124 chr7:125732111-125732122 chr7:125732112-125732123 chr7:125732113-125732122 chr7:125732113-125732122
17	CEBPB	chr7:125731943-125732262	IMR90	lung:	n/a	chr7:125732111-125732124 chr7:125732113-125732122 chr7:125732113-125732122 chr7:125732111-125732124 chr7:125732111-125732122 chr7:125732112-125732123 chr7:125732113-125732122 chr7:125732113-125732122
18	CEBPB	chr7:125579018-125579149	K562	blood:	n/a	chr7:125579076-125579087
19	CEBPB	chr7:125578930-125579240	HepG2	liver:	n/a	chr7:125579076-125579087
20	CEBPB	chr7:125603329-125603585	HepG2	liver:	n/a	chr7:125603411-125603422
21	CEBPB	chr7:125588846-125589425	HepG2	liver:	n/a	chr7:125588880-125588891 chr7:125589282-125589293
22	CEBPB	chr7:125578941-125579239	IMR90	lung:	n/a	chr7:125579076-125579087
23	CEBPB	chr7:125731944-125732277	HepG2	liver:	n/a	chr7:125732111-125732124 chr7:125732113-125732122 chr7:125732113-125732122 chr7:125732111-125732124 chr7:125732111-125732122 chr7:125732112-125732123 chr7:125732113-125732122 chr7:125732113-125732122
24	CEBPB	chr7:125603367-125603565	K562	blood:	n/a	chr7:125603411-125603422
25	CEBPB	chr7:125677488-125677754	HepG2	liver:	n/a	chr7:125677605-125677616
26	CEBPB	chr7:125578989-125579221	A549	lung:	n/a	chr7:125579076-125579087
27	CEBPB	chr7:125700034-125700243	HepG2	liver:	n/a	chr7:125700115-125700126 chr7:125700113-125700126 chr7:125700115-125700126 chr7:125700113-125700124 chr7:125700113-125700126
28	CEBPB	chr7:125694384-125694663	HepG2	liver:	n/a	chr7:125694534-125694545
29	CEBPB	chr7:125603406-125603606	IMR90	lung:	n/a	chr7:125603411-125603422
30	CEBPB	chr7:125654905-125655125	HepG2	liver:	n/a	chr7:125654981-125654994
31	CEBPB	chr7:125641111-125641392	HepG2	liver:	n/a	chr7:125641225-125641236
32	CEBPB	chr7:125719727-125720031	HepG2	liver:	n/a	chr7:125719898-125719909 chr7:125719900-125719911 chr7:125719898-125719911
33	CEBPB	chr7:125654834-125655110	IMR90	lung:	n/a	chr7:125654981-125654994 chr7:125654881-125654892 chr7:125654881-125654892
34	CEBPB	chr7:125699528-125699779	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:125586265-125586333	K562	blood:	n/a	chr7:125586287-125586298 chr7:125586287-125586296
36	CTCF	chr7:125619300-125619450	BE2_C	brain:	n/a	n/a
37	CTCF	chr7:125624885-125625253	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:125664295-125664343	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr7:125609665-125609731	GM12878	blood:	n/a	chr7:125609702-125609723 chr7:125609705-125609713 chr7:125609700-125609718
40	CTCF	chr7:125619292-125619621	GM12878	blood:	n/a	n/a
41	CTCF	chr7:125681756-125681769	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:125681722-125681822	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:125574820-125574970	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr7:125624943-125625110	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr7:125681672-125681830	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:125681710-125681784	GM12891	blood:	n/a	n/a
47	CTCF	chr7:125681770-125681774	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:125609507-125609855	GM12878	blood:	n/a	chr7:125609702-125609723 chr7:125609705-125609713 chr7:125609700-125609718
49	CTCF	chr7:125659070-125659096	GM20000	blood:	n/a	n/a
50	CTCF	chr7:125631281-125631344	GM10248	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
2	chr1:11968074..11970490-chr7:125663203..125664731,2	MCF-7	breast:
3	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
4	chr7:125717773..125720293-chr7:125877157..125879096,2	K562	blood:
5	chr7:125606198..125608530-chr7:125608776..125611774,2	K562	blood:
6	chr3:64659748..64660652-chr7:125742703..125743269,2	MCF-7	breast:
7	chr7:125606198..125608530-chr7:125608776..125611774,2	K562	blood:
8	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
9	chr7:125683918..125686254-chr7:125689679..125692270,2	K562	blood:
10	chr7:125683918..125686254-chr7:125689679..125692270,2	K562	blood:
11	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
12	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
13	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-6	chr7:125573828-125573886	XLOC_006234

Variant related genes	Relation type
ENSG00000221418	TF binding region
ENSG00000201801	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 5630 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5630 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187891519	chr7:125571445-125571446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17149057	chr7:125571446-125571447	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113856718	chr7:125571453-125571454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550154022	chr7:125571576-125571577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568465102	chr7:125571620-125571621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539054215	chr7:125571669-125571670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557531784	chr7:125571724-125571725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572917531	chr7:125571747-125571748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558041239	chr7:125571840-125571841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577116348	chr7:125571908-125571909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193026930	chr7:125571913-125571914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71674577	chr7:125571966-125571967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555573159	chr7:125571983-125571984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573847614	chr7:125572036-125572037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556178767	chr7:125572039-125572040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112450730	chr7:125572049-125572050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541945302	chr7:125572053-125572054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561915970	chr7:125572086-125572087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561948498	chr7:125572091-125572092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546037847	chr7:125572161-125572162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578041917	chr7:125572164-125572165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545435640	chr7:125572232-125572233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184991940	chr7:125572240-125572241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17149059	chr7:125572248-125572249	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549300570	chr7:125572249-125572250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561575587	chr7:125572250-125572251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531788530	chr7:125572294-125572295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201610151	chr7:125572327-125572328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140505067	chr7:125572332-125572333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150422442	chr7:125572359-125572360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539021410	chr7:125572360-125572361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551386870	chr7:125572414-125572415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566431744	chr7:125572454-125572455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143492769	chr7:125572486-125572487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533931523	chr7:125572506-125572507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145197593	chr7:125572528-125572529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149128179	chr7:125572548-125572549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1419556	chr7:125572605-125572606	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538049118	chr7:125572634-125572635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533503552	chr7:125572637-125572638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572971332	chr7:125572763-125572764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7804757	chr7:125572808-125572809	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs578019535	chr7:125572824-125572825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545057651	chr7:125572850-125572851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554178374	chr7:125572869-125572870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572444722	chr7:125572907-125572908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370718807	chr7:125572916-125572917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9649490	chr7:125572917-125572918	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs561232812	chr7:125572932-125572933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9649491	chr7:125573028-125573029	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125566600-125574400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:125567800-125581600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:125568000-125573800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:125568000-125576400	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:125568800-125581400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:125569400-125573600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:125570400-125573400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr7:125571200-125572000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:125571400-125573600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:125572000-125575400	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:125573400-125575000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr7:125573600-125575200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
13	chr7:125573600-125575400	Enhancers	Hela-S3	cervix
14	chr7:125573600-125583200	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr7:125573800-125574000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:125574000-125597400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:125574400-125574800	Enhancers	HMEC	breast
18	chr7:125574400-125575000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:125574600-125575200	Enhancers	NHEK	skin
20	chr7:125575000-125581600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:125575200-125578200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr7:125575400-125577200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:125576400-125577200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:125577200-125577800	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:125577200-125578600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr7:125577800-125578600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr7:125578200-125578600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:125578200-125578800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:125578600-125580400	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:125578600-125581600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:125578800-125579800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr7:125579800-125581200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr7:125580400-125583200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr7:125581200-125583200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr7:125581600-125582200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr7:125581600-125582400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:125581600-125582800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
38	chr7:125582000-125583000	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr7:125582400-125596600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:125582800-125596400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:125583200-125584800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:125583200-125586800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr7:125583200-125596400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr7:125583600-125586000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr7:125584800-125587400	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:125586800-125588000	Genic enhancers	H9 Cell Line	embryonic stem cell
47	chr7:125587200-125587800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:125587400-125590000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:125588000-125593400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:125590000-125595400	Strong transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links