Variant report

Variant	esv2755470
Chromosome Location	chr4:87536515-87613212
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	BATF	chr4:87591451-87591713	GM12878	blood:	n/a	n/a
2	BATF	chr4:87566080-87566330	GM12878	blood:	n/a	n/a
3	BCL11A	chr4:87536626-87536961	GM12878	blood:	n/a	n/a
4	BCL3	chr4:87586206-87586457	GM12878	blood:	n/a	n/a
5	BCL3	chr4:87579173-87579425	GM12878	blood:	n/a	n/a
6	BCL3	chr4:87536670-87537064	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:87543755-87543930	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:87561774-87562073	HepG2	liver:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
9	CEBPB	chr4:87606615-87606811	K562	blood:	n/a	chr4:87606715-87606726
10	CEBPB	chr4:87606590-87606809	K562	blood:	n/a	chr4:87606715-87606726
11	CEBPB	chr4:87597930-87598210	IMR90	lung:	n/a	chr4:87598087-87598098
12	CEBPB	chr4:87606449-87606999	MCF-7	breast:	n/a	chr4:87606715-87606726
13	CEBPB	chr4:87561810-87562062	A549	lung:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
14	CEBPB	chr4:87591749-87592324	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:87591905-87592301	MCF-7	breast:	n/a	n/a
16	CEBPB	chr4:87591889-87592348	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:87586218-87586479	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:87606573-87606879	K562	blood:	n/a	chr4:87606715-87606726
19	CEBPB	chr4:87582343-87582459	A549	lung:	n/a	n/a
20	CEBPB	chr4:87606477-87606917	A549	lung:	n/a	chr4:87606715-87606726
21	CEBPB	chr4:87591893-87592253	A549	lung:	n/a	n/a
22	CEBPB	chr4:87606621-87606821	H1-hESC	embryonic stem cell:	n/a	chr4:87606715-87606726
23	CEBPB	chr4:87591874-87592310	A549	lung:	n/a	n/a
24	CEBPB	chr4:87591918-87592286	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:87606586-87606895	HepG2	liver:	n/a	chr4:87606715-87606726
26	CEBPB	chr4:87561808-87562008	H1-hESC	embryonic stem cell:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
27	CEBPB	chr4:87561770-87562068	IMR90	lung:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
28	CEBPB	chr4:87608844-87608894	K562	blood:	n/a	n/a
29	CEBPB	chr4:87606445-87607040	MCF-7	breast:	n/a	chr4:87606715-87606726
30	CEBPB	chr4:87606526-87606936	A549	lung:	n/a	chr4:87606715-87606726
31	CEBPB	chr4:87597918-87598257	HepG2	liver:	n/a	chr4:87598087-87598098
32	CEBPB	chr4:87591892-87592283	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:87591839-87592346	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:87598026-87598139	K562	blood:	n/a	chr4:87598087-87598098
35	CEBPB	chr4:87606469-87606952	A549	lung:	n/a	chr4:87606715-87606726
36	CEBPB	chr4:87606561-87606885	IMR90	lung:	n/a	chr4:87606715-87606726
37	CEBPB	chr4:87591806-87592268	A549	lung:	n/a	n/a
38	CEBPB	chr4:87598067-87598140	A549	lung:	n/a	chr4:87598087-87598098
39	CEBPB	chr4:87606509-87606997	Hela-S3	cervix:	n/a	chr4:87606715-87606726
40	CEBPB	chr4:87561789-87561992	Hela-S3	cervix:	n/a	chr4:87561879-87561892 chr4:87561940-87561951 chr4:87561938-87561949 chr4:87561938-87561951
41	CHD2	chr4:87556622-87556677	GM12878	blood:	n/a	n/a
42	CREB1	chr4:87537284-87537859	GM12878	blood:	n/a	n/a
43	CREB1	chr4:87536637-87537172	GM12878	blood:	n/a	n/a
44	CTCF	chr4:87574580-87574730	GM12867	blood:	n/a	n/a
45	CTCF	chr4:87574540-87574690	GM12874	blood:	n/a	n/a
46	CTCF	chr4:87574420-87574570	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr4:87574503-87574654	Medullo	brain:	n/a	n/a
48	CTCF	chr4:87574580-87574730	AG10803	skin:	n/a	n/a
49	CTCF	chr4:87541348-87541428	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:87574540-87574690	GM12864	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:87592727..87594779-chr4:87641743..87643865,2	MCF-7	breast:
2	chr4:87592344..87595158-chr4:87604628..87606755,2	K562	blood:
3	chr4:87600177..87602980-chr4:87604745..87606408,2	K562	blood:
4	chr4:87514091..87516787-chr4:87546977..87549306,2	MCF-7	breast:
5	chr4:87534871..87536613-chr4:87547091..87549143,2	K562	blood:
6	chr4:87534871..87536613-chr4:87547091..87549143,2	K562	blood:
7	chr4:87598063..87600452-chr4:87602693..87604467,2	MCF-7	breast:
8	chr4:87514897..87517003-chr4:87606417..87607965,2	MCF-7	breast:
9	chr4:87600177..87602980-chr4:87604745..87606408,2	K562	blood:
10	chr4:87516507..87518409-chr4:87595594..87597208,2	MCF-7	breast:
11	chr4:87574443..87576554-chr4:87578304..87580063,2	MCF-7	breast:
12	chr4:87595555..87598937-chr4:87600350..87602837,3	K562	blood:
13	chr4:87514131..87516860-chr4:87590483..87592754,2	MCF-7	breast:
14	chr4:87513830..87516265-chr4:87582019..87584958,2	MCF-7	breast:
15	chr4:87574188..87575068-chr4:87816619..87817331,3	K562	blood:
16	chr4:87598063..87600452-chr4:87602693..87604467,2	MCF-7	breast:
17	chr4:87595555..87598937-chr4:87600350..87602837,3	K562	blood:
18	chr4:87574443..87576554-chr4:87578304..87580063,2	MCF-7	breast:
19	chr4:87591850..87593506-chr4:87595973..87598861,2	MCF-7	breast:
20	chr4:87530490..87533389-chr4:87533491..87536660,3	MCF-7	breast:
21	chr4:87592344..87595158-chr4:87604628..87606755,2	K562	blood:
22	chr4:87591850..87593506-chr4:87595973..87598861,2	MCF-7	breast:

Variant related genes	Relation type
PTPN13	TF binding region
ENSG00000109339	chromatin interactions
ENSG00000163629	chromatin interactions

Extended variants
information (count: 2507 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17011956	chr4:87536515-87536516	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563827262	chr4:87536557-87536558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535450561	chr4:87536582-87536583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530977913	chr4:87536592-87536593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139857374	chr4:87536677-87536678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564550934	chr4:87536686-87536687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142191098	chr4:87536716-87536717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185747838	chr4:87536785-87536786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567676438	chr4:87536915-87536916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535082682	chr4:87536932-87536933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191296490	chr4:87536948-87536949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568921151	chr4:87536952-87536953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539189343	chr4:87536954-87536955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557930329	chr4:87537000-87537001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112790204	chr4:87537084-87537085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574787363	chr4:87537110-87537111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150768995	chr4:87537112-87537113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555703925	chr4:87537155-87537156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368706178	chr4:87537196-87537197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139125146	chr4:87537202-87537203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563566115	chr4:87537302-87537303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542196968	chr4:87537387-87537388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113860369	chr4:87537422-87537423	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs78342338	chr4:87537437-87537438	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs374097816	chr4:87537482-87537483	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs368196774	chr4:87537518-87537519	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs62308410	chr4:87537562-87537563	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs546841534	chr4:87537630-87537631	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562063567	chr4:87537639-87537640	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529579542	chr4:87537670-87537671	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116007164	chr4:87537701-87537702	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568808373	chr4:87537773-87537774	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533039413	chr4:87537779-87537780	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551198198	chr4:87537797-87537798	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566624900	chr4:87537800-87537801	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs4693778	chr4:87537803-87537804	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201811072	chr4:87537828-87537829	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs112606075	chr4:87537847-87537848	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs372321181	chr4:87537882-87537883	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs537779182	chr4:87537920-87537921	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs557319144	chr4:87537978-87537979	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs575588472	chr4:87537998-87537999	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149957925	chr4:87538010-87538011	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576153055	chr4:87538049-87538050	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186001631	chr4:87538067-87538068	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540439862	chr4:87538075-87538076	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561975738	chr4:87538078-87538079	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs67274037	chr4:87538100-87538101	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147633486	chr4:87538151-87538152	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111460801	chr4:87538177-87538178	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87517000-87536600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:87521400-87546800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr4:87524200-87540800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:87525600-87540200	Weak transcription	NHEK	skin
5	chr4:87526600-87537400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:87531000-87540200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:87531000-87553600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:87532000-87540400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:87532000-87543200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:87532800-87541600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:87532800-87542200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr4:87533000-87540800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:87534000-87542000	Weak transcription	Brain Hippocampus Middle	brain
14	chr4:87534400-87540800	Weak transcription	Brain Anterior Caudate	brain
15	chr4:87534600-87537200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:87535200-87537600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:87535600-87537400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr4:87536000-87536600	Enhancers	Fetal Kidney	kidney
19	chr4:87536200-87536800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr4:87536400-87537200	Enhancers	Brain Cingulate Gyrus	brain
21	chr4:87536400-87540200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:87536600-87536800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:87536600-87547000	Weak transcription	Fetal Kidney	kidney
24	chr4:87536800-87540200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:87536800-87540600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr4:87537200-87542000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:87537400-87538400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:87537600-87538200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:87537800-87538000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:87537800-87538000	Active TSS	Fetal Lung	lung
31	chr4:87538000-87542200	Weak transcription	Fetal Lung	lung
32	chr4:87538000-87546200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:87538200-87540200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:87538400-87542400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:87540000-87540200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr4:87540200-87540400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr4:87540200-87540400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:87540200-87540400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:87540200-87541200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:87540200-87541200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:87540200-87541200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:87540200-87541200	Enhancers	NHEK	skin
43	chr4:87540400-87540600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:87540400-87540800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:87540400-87541400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:87540400-87554000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:87540400-87556200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr4:87540600-87540800	Enhancers	Brain Substantia Nigra	brain
49	chr4:87540600-87542800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:87540800-87541000	Enhancers	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links