Variant report

Variant	rs575220605
Chromosome Location	chr14:103994586-103994587
allele	A/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	NR3C1	chr14:103994442-103994774	A549	lung:	n/a	n/a
2	MAZ	chr14:103994539-103995735	K562	blood:	n/a	n/a
3	CREB1	chr14:103994495-103994914	A549	lung:	n/a	n/a
4	POLR2A	chr14:103994083-103994862	HepG2	liver:	n/a	n/a
5	POLR2A	chr14:103993643-103994932	U87	brain:	n/a	n/a
6	POLR2A	chr14:103993629-103994989	GM12878	blood:	n/a	n/a
7	ELF1	chr14:103994419-103997638	MCF-7	breast:	n/a	chr14:103995523-103995532 chr14:103995487-103995496 chr14:103995544-103995553 chr14:103995522-103995533 chr14:103995540-103995552 chr14:103995488-103995500 chr14:103995541-103995550
8	MTA3	chr14:103994458-103996055	GM12878	blood:	n/a	n/a
9	POLR2A	chr14:103994449-103996359	MCF10A-Er-Src	breast:	n/a	n/a
10	CHD2	chr14:103994507-103994707	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr14:103994080-103996288	SK-N-MC	brain:	n/a	n/a
12	HEY1	chr14:103994239-103995825	HepG2	liver:	n/a	chr14:103995540-103995555 chr14:103995539-103995554
13	MAX	chr14:103994457-103996062	HepG2	liver:	n/a	chr14:103995561-103995571
14	MAX	chr14:103994440-103996416	A549	lung:	n/a	chr14:103995561-103995571
15	POLR2A	chr14:103994574-103994645	HUVEC	blood vessel:	n/a	n/a
16	NR3C1	chr14:103994478-103994691	A549	lung:	n/a	n/a
17	POLR2A	chr14:103993577-103995852	U87	brain:	n/a	n/a
18	CHD2	chr14:103994556-103994752	GM12878	blood:	n/a	n/a
19	ESRRA	chr14:103994512-103996444	GM12878	blood:	n/a	chr14:103994819-103994832 chr14:103995633-103995652 chr14:103995617-103995630 chr14:103994792-103994806 chr14:103994787-103994806 chr14:103995633-103995647 chr14:103995632-103995648 chr14:103995638-103995647 chr14:103995628-103995647
20	ZNF263	chr14:103994420-103994880	HEK293-T-REx	kidney:	n/a	n/a
21	POLR2A	chr14:103994456-103994802	HepG2	liver:	n/a	n/a
22	NRF1	chr14:103994558-103994728	GM12878	blood:	n/a	n/a
23	POLR2A	chr14:103994096-103996062	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr14:103993503-103995855	U87	brain:	n/a	n/a
25	MXI1	chr14:103994392-103997122	SK-N-SH	brain:	n/a	n/a
26	MXI1	chr14:103994501-103997427	IMR90	lung:	n/a	n/a
27	POLR2A	chr14:103990643-103996520	HepG2	liver:	n/a	n/a
28	POLR2A	chr14:103994336-103996408	K562	blood:	n/a	n/a
29	POLR2A	chr14:103994461-103994952	A549	lung:	n/a	n/a
30	MAX	chr14:103994246-103996064	HepG2	liver:	n/a	chr14:103995561-103995571
31	RCOR1	chr14:103994493-103994671	K562	blood:	n/a	n/a
32	MAZ	chr14:103994550-103995797	IMR90	lung:	n/a	n/a
33	POLR2A	chr14:103994554-103995756	K562	blood:	n/a	n/a
34	POLR2A	chr14:103994496-103994669	ProgFib	skin:	n/a	n/a
35	POLR2A	chr14:103994531-103994857	MCF-7	breast:	n/a	n/a
36	POLR2A	chr14:103994388-103995782	HepG2	liver:	n/a	n/a
37	POLR2A	chr14:103994461-103994901	A549	lung:	n/a	n/a
38	POLR2A	chr14:103994558-103994666	MCF-7	breast:	n/a	n/a
39	POLR2A	chr14:103994394-103994931	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103851236..103854697-chr14:103993929..103996210,3	MCF-7	breast:
2	chr14:103992721..103998040-chr14:104027797..104030842,4	MCF-7	breast:
3	chr14:103993654..103996154-chr14:104180669..104183057,2	K562	blood:
4	chr14:103992666..103995489-chr14:104177229..104179572,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CKB-1	chr14:103991347-103995409	ENSG00000260285.1

Variant related genes	Relation type
TRMT61A	TF binding region
ENSG00000166170	Chromatin interaction
ENSG00000224997	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000126214	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
3	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1044967	chr14:103954727-104007051	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv1807091	chr14:103956182-104020454	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	esv1835824	chr14:103956182-104020454	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv902297	chr14:103956182-104061646	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
8	nsv902298	chr14:103959289-104061646	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
9	nsv902299	chr14:103967504-104061646	Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
10	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
11	esv1834605	chr14:103969909-104003091	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
12	nsv902301	chr14:103979953-104003094	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	esv1850440	chr14:103979953-104007555	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv902302	chr14:103979953-104018455	Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv902303	chr14:103979953-104034746	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
16	nsv902304	chr14:103979953-104061646	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
17	nsv902305	chr14:103979953-104073551	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
18	nsv827068	chr14:103982866-104021347	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv902306	chr14:103984294-104003094	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	esv1835145	chr14:103984294-104014935	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
21	nsv902307	chr14:103986155-104003094	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	esv1824096	chr14:103986255-103999371	Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
23	esv1842368	chr14:103986255-103999371	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
24	esv1834274	chr14:103987140-103996205	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
25	esv1834291	chr14:103987140-103999371	Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
26	esv1839917	chr14:103987140-103999371	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
27	esv1845597	chr14:103987140-103999371	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
28	esv1851656	chr14:103987140-104007555	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
29	esv1839595	chr14:103987140-104034746	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
30	esv1809007	chr14:103988059-103999371	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
31	esv1818214	chr14:103988059-103999371	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
32	esv1837939	chr14:103988059-103999371	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
33	esv1846909	chr14:103988059-103999371	Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
34	esv1794331	chr14:103988059-104004311	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
35	nsv566020	chr14:103989279-103996396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
36	nsv566021	chr14:103989639-104012982	Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
37	esv1819920	chr14:103989971-104018096	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
38	nsv9170	chr14:103994260-104017971	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103989600-103994600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr14:103989800-103994600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr14:103990200-103994600	Enhancers	Pancreas	Pancrea
4	chr14:103990800-103994600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:103990800-103994600	Enhancers	Fetal Stomach	stomach
6	chr14:103991000-103994600	Enhancers	Liver	Liver
7	chr14:103991000-103994600	Enhancers	Fetal Muscle Leg	muscle
8	chr14:103991400-103994600	Enhancers	Fetal Muscle Trunk	muscle
9	chr14:103991800-103994800	Enhancers	Fetal Heart	heart
10	chr14:103991800-103994800	Enhancers	Placenta	Placenta
11	chr14:103992200-103994600	Enhancers	Right Ventricle	heart
12	chr14:103992200-103995000	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr14:103992400-103994600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:103992400-103994600	Enhancers	Lung	lung
15	chr14:103992400-103994800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr14:103992400-103995000	Enhancers	Spleen	Spleen
17	chr14:103992600-103994600	Enhancers	Primary B cells from cord blood	blood
18	chr14:103992600-103994600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:103992600-103994800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr14:103992800-103994600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:103992800-103994800	Enhancers	Primary B cells from peripheral blood	blood
22	chr14:103993000-103994600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr14:103993000-103994600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
24	chr14:103993000-103994800	Enhancers	Primary T cells fromperipheralblood	blood
25	chr14:103993200-103994600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:103993200-103994600	Enhancers	Colon Smooth Muscle	Colon
27	chr14:103993200-103994600	Enhancers	Placenta Amnion	Placenta Amnion
28	chr14:103993200-103995200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
29	chr14:103993400-103994600	Enhancers	HSMM	muscle
30	chr14:103993400-103994600	Enhancers	NHEK	skin
31	chr14:103993400-103995200	Flanking Active TSS	Osteobl	bone
32	chr14:103993600-103994600	Enhancers	Gastric	stomach
33	chr14:103993600-103994600	Enhancers	Stomach Mucosa	stomach
34	chr14:103993600-103994600	Enhancers	NH-A	brain
35	chr14:103993600-103994600	Enhancers	NHLF	lung
36	chr14:103993600-103995000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:103993600-103995200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr14:103993600-103995200	Flanking Active TSS	GM12878-XiMat	blood
39	chr14:103993800-103994600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr14:103993800-103994600	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr14:103993800-103994600	Enhancers	Brain Cingulate Gyrus	brain
42	chr14:103993800-103994600	Flanking Active TSS	HepG2	liver
43	chr14:103993800-103994800	Enhancers	Fetal Brain Male	brain
44	chr14:103994000-103994600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr14:103994000-103994600	Enhancers	Primary hematopoietic stem cells	blood
46	chr14:103994000-103994600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr14:103994000-103994600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr14:103994000-103994600	Enhancers	Brain Angular Gyrus	brain
49	chr14:103994000-103994600	Enhancers	Esophagus	oesophagus
50	chr14:103994000-103994600	Enhancers	Left Ventricle	heart

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