Variant report

Variant	esv1814392
Chromosome Location	chr1:62433100-62448451
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	ATF3	chr1:62433476-62433726	K562	blood:	n/a	n/a
2	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
4	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
5	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
6	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
7	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
8	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
10	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
11	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
13	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr1:62448125-62448179	GM12878	blood:	n/a	n/a
15	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
17	CUX1	chr1:62433241-62433259	K562	blood:	n/a	n/a
18	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
20	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
21	EP300	chr1:62433418-62433730	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
22	EP300	chr1:62433430-62433743	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
23	FOS	chr1:62446342-62446638	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
24	FOS	chr1:62440032-62440239	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:62440055-62440275	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:62440039-62440275	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:62446306-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
28	FOS	chr1:62438816-62439128	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:62440074-62440275	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:62446306-62446560	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
33	FOS	chr1:62446297-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
34	FOXA1	chr1:62441400-62441592	T-47D	breast:	n/a	n/a
35	FOXA1	chr1:62441344-62441639	T-47D	breast:	n/a	n/a
36	FOXP2	chr1:62446307-62446517	SK-N-MC	brain:	n/a	n/a
37	GATA2	chr1:62433432-62433718	SH-SY5Y	brain:	n/a	n/a
38	GATA2	chr1:62445408-62445710	K562	blood:	n/a	n/a
39	GATA3	chr1:62441303-62441694	T-47D	breast:	n/a	n/a
40	GATA3	chr1:62432959-62433967	SK-N-SH	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433136-62433157 chr1:62433138-62433154 chr1:62433141-62433151 chr1:62433143-62433150
41	GATA3	chr1:62433139-62433695	SH-SY5Y	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433141-62433151 chr1:62433143-62433150
42	GATA3	chr1:62448112-62448183	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr1:62433236-62433904	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr1:62441311-62441758	T-47D	breast:	n/a	n/a
45	JUND	chr1:62433370-62433855	SK-N-SH	brain:	n/a	chr1:62433503-62433512
46	JUND	chr1:62433358-62433932	SK-N-SH	brain:	n/a	chr1:62433503-62433512
47	KAP1	chr1:62439825-62440303	U2OS	brain:	n/a	n/a
48	KAP1	chr1:62439821-62440264	HEK293	kidney:	n/a	n/a
49	KAP1	chr1:62444519-62445549	U2OS	brain:	n/a	n/a
50	KAP1	chr1:62444569-62445769	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	U87	brain:	n/a
2	chr1:62445916-62445966	GM12892	blood:	n/a
3	chr1:62445916-62445966	NT2-D1	testis:	n/a
4	chr1:62445916-62445966	HNPCEpiC	eye:	n/a
5	chr1:62445916-62445966	H1-hESC	embryonic stem cell:	embryo
6	chr1:62445916-62445966	HUVEC	blood vessel:	n/a
7	chr1:62445916-62445966	Hepatocyte	liver:	n/a
8	chr1:62445916-62445966	GM12878	blood:	n/a
9	chr1:62445916-62445966	A549	lung:	n/a
10	chr1:62445916-62445966	Caco-2	colon:	n/a
11	chr1:62445916-62445966	HEEpiC	esophagus:	n/a
12	chr1:62445916-62445966	HL-60	blood:	n/a
13	chr1:62445916-62445966	HCT-116	colon:	n/a
14	chr1:62445916-62445966	SAEC	small airway:	n/a
15	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
16	chr1:62445916-62445966	LNCaP	prostate:	n/a
17	chr1:62445916-62445966	AG04450	lung:	fetal
18	chr1:62445916-62445966	ProgFib	skin:	n/a
19	chr1:62445916-62445966	PANC-1	pancreas:	n/a
20	chr1:62445916-62445966	MCF-7	breast:	n/a
21	chr1:62445916-62445966	K562	blood:	n/a
22	chr1:62445916-62445966	Jurkat	blood:	n/a
23	chr1:62445916-62445966	SK-N-SH	brain:	n/a
24	chr1:62445916-62445966	AG04449	skin:	fetal
25	chr1:62445916-62445966	HCF	heart:	n/a
26	chr1:62445916-62445966	CMK	blood:	n/a
27	chr1:62445916-62445966	RPTEC	kidney:	n/a
28	chr1:62445916-62445966	AG10803	skin:	n/a
29	chr1:62445916-62445966	HMEC	breast:	n/a
30	chr1:62445916-62445966	AG09309	skin:	n/a
31	chr1:62445916-62445966	GM12891	blood:	n/a
32	chr1:62445916-62445966	HepG2	liver:	n/a
33	chr1:62445916-62445966	HIPEpiC	eye:	n/a
34	chr1:62445916-62445966	GM19239	blood:	n/a
35	chr1:62445916-62445966	PrEC	prostate:	n/a
36	chr1:62445916-62445966	ECC-1	luminal epithelium:	n/a
37	chr1:62445916-62445966	SK-N-MC	brain:	n/a
38	chr1:62445916-62445966	HEK293	kidney:	embryo
39	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
40	chr1:62445916-62445966	GM06990	blood:	n/a
41	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:62445916-62445966	HCPEpiC	choroid plexus:	n/a
43	chr1:62445916-62445966	SKMC	muscle:	n/a
44	chr1:62445916-62445966	AG09319	gingival:	n/a
45	chr1:62445916-62445966	BJ	skin:	n/a
46	chr1:62445916-62445966	NB4	blood:	n/a
47	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
48	chr1:62445916-62445966	HCM	heart:	n/a
49	chr1:62445916-62445966	IMR90	lung:	fetal
50	chr1:62445916-62445966	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
2	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island

Extended variants
information (count: 550 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2498967	chr1:62433100-62433101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556363262	chr1:62433102-62433103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577925025	chr1:62433128-62433129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545079321	chr1:62433130-62433131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567612828	chr1:62433244-62433245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560190499	chr1:62433394-62433395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187037974	chr1:62433404-62433405	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191841180	chr1:62433545-62433546	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183611547	chr1:62433551-62433552	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531848717	chr1:62433666-62433667	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550068017	chr1:62433702-62433703	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114356652	chr1:62433731-62433732	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188263256	chr1:62433760-62433761	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547714760	chr1:62433791-62433792	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138806142	chr1:62433807-62433808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182028655	chr1:62433809-62433810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114795744	chr1:62433821-62433822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570082153	chr1:62433857-62433858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185746138	chr1:62433939-62433940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189882243	chr1:62433999-62434000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17385742	chr1:62434037-62434038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs377203463	chr1:62434096-62434097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149361423	chr1:62434097-62434098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12735117	chr1:62434137-62434138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114338924	chr1:62434149-62434150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560898045	chr1:62434200-62434201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181933921	chr1:62434237-62434238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543060672	chr1:62434294-62434295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112723971	chr1:62434330-62434331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185545370	chr1:62434331-62434332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534132830	chr1:62434339-62434340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532700169	chr1:62434352-62434353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144606507	chr1:62434379-62434380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555637145	chr1:62434395-62434396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190217486	chr1:62434396-62434397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548402800	chr1:62434402-62434403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570018811	chr1:62434407-62434408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370105938	chr1:62434413-62434414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538395673	chr1:62434493-62434494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116570423	chr1:62434534-62434535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4915791	chr1:62434604-62434605	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs113929696	chr1:62434611-62434612	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs538586605	chr1:62434681-62434682	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs115974867	chr1:62434692-62434693	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs181435042	chr1:62434733-62434734	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs367998702	chr1:62434749-62434750	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs572154373	chr1:62434793-62434794	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs2990509	chr1:62434806-62434807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555766595	chr1:62434847-62434848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142595608	chr1:62434918-62434919	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
2	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
6	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
7	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
10	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
11	chr1:62423400-62433600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:62423600-62433800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr1:62424200-62436600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
15	chr1:62424800-62438200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:62425000-62441400	Weak transcription	Stomach Mucosa	stomach
17	chr1:62430600-62435400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:62430600-62442200	Weak transcription	Fetal Intestine Small	intestine
19	chr1:62432000-62433400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:62432000-62435600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr1:62432200-62439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:62432400-62433600	Enhancers	NHEK	skin
23	chr1:62432400-62434000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:62432800-62433200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:62432800-62433400	Enhancers	HMEC	breast
26	chr1:62432800-62433600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:62432800-62433800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr1:62432800-62433800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:62433000-62434000	Enhancers	NH-A	brain
30	chr1:62433200-62433600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:62433200-62433800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:62433200-62433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:62433200-62433800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:62433200-62433800	Enhancers	Fetal Heart	heart
35	chr1:62433200-62434000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:62433400-62433800	Genic enhancers	HMEC	breast
37	chr1:62433400-62434000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:62433400-62439200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:62433600-62433800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:62433600-62434600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr1:62433600-62456800	Weak transcription	NHEK	skin
42	chr1:62433800-62434000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:62433800-62438600	Weak transcription	HMEC	breast
44	chr1:62433800-62444800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr1:62433800-62445400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:62434000-62457000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:62434600-62434800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr1:62434800-62444800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:62435400-62435800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:62435800-62436000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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