Variant report

Variant	rs2984716
Chromosome Location	chr14:24505097-24505098
allele	A/C/G
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	TAF1	chr14:24504822-24506190	HepG2	liver:	n/a	n/a
2	CTCF	chr14:24505040-24505190	HEK293	kidney:	n/a	n/a
3	POLR2A	chr14:24505025-24506196	A549	lung:	n/a	n/a
4	POU2F2	chr14:24504909-24505541	GM12878	blood:	n/a	chr14:24504990-24505004
5	POLR2A	chr14:24504890-24506185	HepG2	liver:	n/a	n/a
6	JUND	chr14:24504937-24506264	HepG2	liver:	n/a	chr14:24505835-24505843
7	CTCF	chr14:24505040-24505190	HMEC	breast:	n/a	n/a
8	CTCF	chr14:24505020-24505170	NHEK	skin:	n/a	n/a
9	SIN3AK20	chr14:24504926-24505114	HepG2	liver:	n/a	n/a
10	POLR2A	chr14:24504987-24506333	GM12892	blood:	n/a	n/a
11	CTCF	chr14:24505020-24505170	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr14:24505040-24505190	Caco-2	colon:	n/a	n/a
13	SPI1	chr14:24504942-24505104	K562	blood:	n/a	chr14:24505054-24505067
14	SP1	chr14:24504070-24506291	HepG2	liver:	n/a	chr14:24505596-24505610 chr14:24506258-24506267 chr14:24505023-24505037 chr14:24506256-24506268 chr14:24505429-24505441 chr14:24506256-24506268 chr14:24506257-24506267 chr14:24505641-24505655 chr14:24505132-24505146 chr14:24505429-24505441 chr14:24505431-24505440 chr14:24505600-24505609 chr14:24505430-24505439 chr14:24506257-24506271
15	CTCF	chr14:24505020-24505170	HCT-116	colon:	n/a	n/a
16	CTCF	chr14:24504983-24506449	SK-N-SH	brain:	n/a	chr14:24505206-24505215 chr14:24505418-24505431 chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
17	RAD21	chr14:24505029-24505351	H1-hESC	embryonic stem cell:	n/a	chr14:24505207-24505216 chr14:24505198-24505217
18	CTCF	chr14:24505020-24505170	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:24505080-24505230	HFF	foreskin:	n/a	chr14:24505206-24505215
20	CTCF	chr14:24505060-24505210	A549	lung:	n/a	n/a
21	CTCF	chr14:24505040-24505190	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr14:24505060-24505210	MCF-7	breast:	n/a	n/a
23	POLR2A	chr14:24504974-24506349	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr14:24505022-24505238	H1-hESC	embryonic stem cell:	n/a	chr14:24505206-24505215
25	CTCF	chr14:24505000-24505150	NHEK	skin:	n/a	n/a
26	CTCF	chr14:24505040-24505190	GM12874	blood:	n/a	n/a
27	FOSL2	chr14:24504803-24506841	HepG2	liver:	n/a	chr14:24505835-24505843 chr14:24506578-24506590
28	CTCF	chr14:24505060-24505210	GM12872	blood:	n/a	n/a
29	SPI1	chr14:24504930-24505188	GM12878	blood:	n/a	chr14:24505054-24505067 chr14:24505137-24505150
30	CTCF	chr14:24505040-24505190	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr14:24505060-24505210	GM12866	blood:	n/a	n/a
32	CTCF	chr14:24505020-24505170	GM12873	blood:	n/a	n/a
33	RAD21	chr14:24504997-24506479	SK-N-SH	brain:	n/a	chr14:24505207-24505216 chr14:24506038-24506052 chr14:24506120-24506139 chr14:24505419-24505432 chr14:24505428-24505438 chr14:24505198-24505217
34	EBF1	chr14:24504937-24505793	GM12878	blood:	n/a	n/a
35	TCF7L2	chr14:24505075-24505746	HEK293	kidney:	n/a	chr14:24505466-24505482 chr14:24505467-24505481
36	MYBL2	chr14:24505018-24506478	HepG2	liver:	n/a	n/a
37	MYBL2	chr14:24505047-24506395	HepG2	liver:	n/a	n/a
38	CTCF	chr14:24505040-24505190	RPTEC	kidney:	n/a	n/a
39	POLR2A	chr14:24504954-24505302	A549	lung:	n/a	n/a
40	CTCF	chr14:24505040-24505190	HCT-116	colon:	n/a	n/a
41	CTCF	chr14:24505000-24505150	GM12878	blood:	n/a	n/a
42	CTCF	chr14:24505040-24505190	HepG2	liver:	n/a	n/a
43	CTCF	chr14:24505040-24505190	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr14:24505060-24505210	GM12873	blood:	n/a	n/a
45	HEY1	chr14:24505090-24506314	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
2	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
3	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
4	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000225766	TF binding region
ENSG00000157379	Chromatin interaction
ENSG00000196943	Chromatin interaction
ENSG00000100897	Chromatin interaction
ENSG00000100889	Chromatin interaction
ENSG00000215256	Chromatin interaction
ENSG00000157326	Chromatin interaction
ENSG00000129535	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1043650	1.00[AFR][1000 genomes]
rs45592432	1.00[AFR][1000 genomes]
rs45596131	1.00[AMR][1000 genomes]
rs55643821	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55664822	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55691977	1.00[AMR][1000 genomes]
rs55696718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55774579	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55777341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55795553	0.87[EUR][1000 genomes]
rs55895464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55911718	0.84[EUR][1000 genomes]
rs55933233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55986585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56013927	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56021847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56079821	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs56145320	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs56166780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56171184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56239015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999785	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61999794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999797	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999798	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs61999799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999850	1.00[AFR][1000 genomes]
rs61999852	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61999855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61999856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62000761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62000792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62000814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62000817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62000818	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7150459	1.00[EUR][1000 genomes]
rs7158037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7160290	0.96[EUR][1000 genomes]
rs72692113	1.00[AFR][1000 genomes]
rs72692114	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs72692115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72692116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72692118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72692119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72692120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72692121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72692132	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72692141	1.00[AFR][1000 genomes]
rs8013243	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3405661	chr14:24189883-24670942	Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
2	nsv1217	chr14:24400565-24512689	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1049316	chr14:24405420-24583724	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv541999	chr14:24405420-24583724	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	esv2761633	chr14:24423582-24513917	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv564047	chr14:24428509-24525634	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv901497	chr14:24429249-24514449	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1052180	chr14:24429298-24555710	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	esv33403	chr14:24429613-24505105	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv826901	chr14:24457315-24508468	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1048292	chr14:24474511-24513905	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
12	nsv9126	chr14:24475840-24505714	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
13	nsv1049192	chr14:24478882-24519250	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
14	nsv1037929	chr14:24478882-24522447	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
15	nsv1052857	chr14:24479375-24513905	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
16	nsv1047042	chr14:24484459-24513905	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
17	nsv1038839	chr14:24488131-24510197	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
18	nsv1044763	chr14:24488131-24513905	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
19	nsv1051893	chr14:24488131-24519250	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
20	nsv1043854	chr14:24488131-24522447	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
21	nsv1049849	chr14:24488384-24513905	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
22	nsv516023	chr14:24489605-24550224	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
23	nsv1038278	chr14:24494063-24513905	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
24	nsv1042507	chr14:24494153-24513905	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
25	nsv983808	chr14:24503854-24523979	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24501800-24505200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:24501800-24505200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr14:24502000-24505200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:24502000-24505200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr14:24502400-24505400	Weak transcription	HMEC	breast
6	chr14:24502600-24505200	Weak transcription	Osteobl	bone
7	chr14:24502600-24505400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:24503000-24505400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:24503400-24505200	Enhancers	Fetal Thymus	thymus
10	chr14:24503600-24505200	Weak transcription	Psoas Muscle	Psoas
11	chr14:24503600-24505400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr14:24503600-24505600	Weak transcription	NHLF	lung
13	chr14:24503800-24505200	Enhancers	Fetal Intestine Large	intestine
14	chr14:24503800-24505200	Weak transcription	Placenta	Placenta
15	chr14:24503800-24505400	Weak transcription	Esophagus	oesophagus
16	chr14:24503800-24505600	Weak transcription	NHDF-Ad	bronchial
17	chr14:24504000-24505200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:24504000-24505200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:24504000-24505200	Weak transcription	Brain Angular Gyrus	brain
20	chr14:24504000-24505400	Weak transcription	Primary B cells from cord blood	blood
21	chr14:24504200-24505200	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr14:24504400-24505200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:24504600-24505400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr14:24504600-24505400	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr14:24504800-24505200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:24504800-24505200	Enhancers	Fetal Muscle Leg	muscle
27	chr14:24505000-24505200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr14:24505000-24505200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr14:24505000-24505200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:24505000-24505200	Enhancers	Primary T cells fromperipheralblood	blood
31	chr14:24505000-24505200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr14:24505000-24505200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:24505000-24505200	Enhancers	Adipose Nuclei	Adipose
34	chr14:24505000-24505200	Enhancers	Liver	Liver
35	chr14:24505000-24505200	Enhancers	Brain Cingulate Gyrus	brain
36	chr14:24505000-24505200	Enhancers	Brain Germinal Matrix	brain
37	chr14:24505000-24505200	Enhancers	Brain Hippocampus Middle	brain
38	chr14:24505000-24505200	Enhancers	Colonic Mucosa	Colon
39	chr14:24505000-24505200	Enhancers	Duodenum Mucosa	Duodenum
40	chr14:24505000-24505200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr14:24505000-24505200	Flanking Active TSS	Fetal Lung	lung
42	chr14:24505000-24505200	Enhancers	Pancreas	Pancrea
43	chr14:24505000-24505200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr14:24505000-24505200	Enhancers	Right Ventricle	heart
45	chr14:24505000-24505200	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr14:24505000-24505200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr14:24505000-24505200	Flanking Active TSS	Hela-S3	cervix
48	chr14:24505000-24505200	Flanking Active TSS	HepG2	liver
49	chr14:24505000-24505400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr14:24505000-24505400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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