Variant report

Variant	nsv1037902
Chromosome Location	chr14:22229021-22354103
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	ARID3A	chr14:22314485-22314711	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:22236446-22236646	K562	blood:	n/a	n/a
3	BACH1	chr14:22239915-22240160	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:22336665-22336765	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:22236359-22236692	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:22236428-22236693	K562	blood:	n/a	n/a
7	BHLHE40	chr14:22328457-22328580	HepG2	liver:	n/a	n/a
8	BRCA1	chr14:22320309-22320440	HepG2	liver:	n/a	n/a
9	CBX3	chr14:22314483-22314815	HCT-116	colon:	n/a	n/a
10	CEBPB	chr14:22331634-22331889	IMR90	lung:	n/a	chr14:22331764-22331775
11	CEBPB	chr14:22270575-22270843	HepG2	liver:	n/a	chr14:22270690-22270701
12	CEBPB	chr14:22331605-22331904	HepG2	liver:	n/a	chr14:22331764-22331775
13	CEBPB	chr14:22249926-22250066	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:22335185-22335344	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:22314496-22314592	A549	lung:	n/a	n/a
16	CEBPB	chr14:22331641-22331879	A549	lung:	n/a	chr14:22331764-22331775
17	CEBPB	chr14:22278968-22279088	HepG2	liver:	n/a	chr14:22279034-22279045
18	CEBPB	chr14:22249065-22249134	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:22331741-22331789	K562	blood:	n/a	chr14:22331764-22331775
20	CHD2	chr14:22320385-22320589	GM12878	blood:	n/a	n/a
21	CTCF	chr14:22328500-22328650	BJ	skin:	n/a	n/a
22	CTCF	chr14:22293400-22293550	GM12866	blood:	n/a	chr14:22293481-22293499 chr14:22293515-22293523 chr14:22293483-22293504
23	CTCF	chr14:22336760-22336910	HAc	cerebellar:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
24	CTCF	chr14:22337420-22337570	GM12872	blood:	n/a	n/a
25	CTCF	chr14:22328393-22328530	Fibrobl	skin:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
26	CTCF	chr14:22236460-22236610	Caco-2	colon:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
27	CTCF	chr14:22314180-22314330	NHEK	skin:	n/a	n/a
28	CTCF	chr14:22336703-22336905	SK-N-SH_RA	brain:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
29	CTCF	chr14:22293382-22293647	A549	lung:	n/a	chr14:22293481-22293499 chr14:22293515-22293523 chr14:22293483-22293504
30	CTCF	chr14:22314497-22314778	Medullo	brain:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
31	CTCF	chr14:22314580-22314730	AG09309	skin:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
32	CTCF	chr14:22236540-22236690	HA-sp	spinal cord:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
33	CTCF	chr14:22314240-22314390	HPF	lung:	n/a	n/a
34	CTCF	chr14:22304500-22304650	GM12873	blood:	n/a	n/a
35	CTCF	chr14:22314160-22314310	GM06990	blood:	n/a	n/a
36	CTCF	chr14:22293440-22293590	GM12892	blood:	n/a	chr14:22293481-22293499 chr14:22293515-22293523 chr14:22293483-22293504
37	CTCF	chr14:22236440-22236590	HRE	kidney:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
38	CTCF	chr14:22320749-22320838	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr14:22328420-22328570	HFF	foreskin:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
40	CTCF	chr14:22320340-22320490	HBMEC	blood vessel:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
41	CTCF	chr14:22314500-22314650	SAEC	small airway:	n/a	chr14:22314636-22314645 chr14:22314638-22314648
42	CTCF	chr14:22265076-22265457	MCF-7	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
43	CTCF	chr14:22293380-22293530	HPAF	blood vessel:	n/a	chr14:22293481-22293499 chr14:22293515-22293523 chr14:22293483-22293504
44	CTCF	chr14:22336760-22336910	SAEC	small airway:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
45	CTCF	chr14:22236491-22236663	GM19239	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
46	CTCF	chr14:22236520-22236648	Fibrobl	skin:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
47	CTCF	chr14:22293420-22293570	GM12870	blood:	n/a	chr14:22293481-22293499 chr14:22293515-22293523 chr14:22293483-22293504
48	CTCF	chr14:22320360-22320510	GM12865	blood:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
49	CTCF	chr14:22314520-22314670	GM12866	blood:	n/a	chr14:22314635-22314656 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
50	CTCF	chr14:22314510-22314751	K562	blood:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22236018-22236068	HMEC	breast:	n/a
2	chr14:22314416-22314466	HCPEpiC	choroid plexus:	n/a
3	chr14:22336403-22336453	HIPEpiC	eye:	n/a
4	chr14:22314416-22314466	A549	lung:	n/a
5	chr14:22320448-22320498	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:22309073-22309123	T-47D	breast:	n/a
7	chr14:22314958-22315008	NH-A	brain:	n/a
8	chr14:22314540-22314590	SK-N-MC	brain:	n/a
9	chr14:22279816-22279866	SK-N-SH_RA	brain:	n/a
10	chr14:22236018-22236068	HL-60	blood:	n/a
11	chr14:22265369-22265419	HIPEpiC	eye:	n/a
12	chr14:22314958-22315008	T-47D	breast:	n/a
13	chr14:22320448-22320498	SK-N-SH	brain:	n/a
14	chr14:22336334-22336384	HAEpiC	amniotic membrane:	n/a
15	chr14:22236018-22236068	Caco-2	colon:	n/a
16	chr14:22336334-22336384	HUVEC	blood vessel:	n/a
17	chr14:22265369-22265419	Jurkat	blood:	n/a
18	chr14:22314682-22314732	HUVEC	blood vessel:	n/a
19	chr14:22320101-22320151	HAEpiC	amniotic membrane:	n/a
20	chr14:22241537-22241587	NH-A	brain:	n/a
21	chr14:22292347-22292397	SK-N-SH	brain:	n/a
22	chr14:22314682-22314732	A549	lung:	n/a
23	chr14:22292347-22292397	ECC-1	luminal epithelium:	n/a
24	chr14:22320448-22320498	NT2-D1	testis:	n/a
25	chr14:22236519-22236569	AG09319	gingival:	n/a
26	chr14:22265369-22265419	CMK	blood:	n/a
27	chr14:22320101-22320151	T-47D	breast:	n/a
28	chr14:22336403-22336453	IMR90	lung:	fetal
29	chr14:22241537-22241587	ProgFib	skin:	n/a
30	chr14:22320448-22320498	HIPEpiC	eye:	n/a
31	chr14:22314958-22315008	HMEC	breast:	n/a
32	chr14:22336334-22336384	HRCEpiC	kidney:	n/a
33	chr14:22236519-22236569	HCF	heart:	n/a
34	chr14:22320101-22320151	K562	blood:	n/a
35	chr14:22265369-22265419	AG09309	skin:	n/a
36	chr14:22320101-22320151	H1-hESC	embryonic stem cell:	embryo
37	chr14:22320448-22320498	Caco-2	colon:	n/a
38	chr14:22320101-22320151	BE2_C	brain:	n/a
39	chr14:22320101-22320151	Hela-S3	cervix:	n/a
40	chr14:22314682-22314732	Jurkat	blood:	n/a
41	chr14:22314416-22314466	NHDF-neo	bronchial:	n/a
42	chr14:22320448-22320498	MCF-7	breast:	n/a
43	chr14:22292347-22292397	HNPCEpiC	eye:	n/a
44	chr14:22241537-22241587	HCPEpiC	choroid plexus:	n/a
45	chr14:22320326-22320376	GM12891	blood:	n/a
46	chr14:22314416-22314466	GM12892	blood:	n/a
47	chr14:22315066-22315116	ECC-1	luminal epithelium:	n/a
48	chr14:22336334-22336384	PrEC	prostate:	n/a
49	chr14:22314416-22314466	LNCaP	prostate:	n/a
50	chr14:22314958-22315008	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22327903..22328851-chr14:22336403..22337266,2	MCF-7	breast:
2	chr14:22319960..22320506-chr14:22370012..22371430,7	MCF-7	breast:
3	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:
4	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
5	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
6	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
7	chr14:22293105..22294016-chr14:22319903..22320481,2	MCF-7	breast:
8	chr14:22264815..22265316-chr14:22293406..22294027,2	MCF-7	breast:
9	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
10	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
11	chr14:22217192..22217714-chr14:22336654..22337322,2	MCF-7	breast:
12	chr12:122491977..122492787-chr14:22328270..22328892,2	MCF-7	breast:
13	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
14	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:
15	chr14:22236090..22236721-chr14:22293035..22293909,3	MCF-7	breast:
16	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:
17	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22337290-22337543	NONHSAT035709
2	lnc-OR4E2-2	chr14:22297937-22298223	NONHSAT035707
3	lnc-OR4E2-2	chr14:22297692-22297743	NONHSAT035707
4	lnc-OR10G2-5	chr14:22320548-22320780	NONHSAT035708
5	lnc-AE000662.92.1-10	chr14:22237068-22237313	NONHSAT035705
6	lnc-OR10G2-5	chr14:22320890-22321003	NONHSAT035708

Variant related genes	Relation type
TRAV8-2	TF binding region
TRAV6	TF binding region
TRAV8-1	TF binding region
ENSG00000222776	TF binding region
TRAV13-1	TF binding region
TRAV7	TF binding region
TRAV10	TF binding region
TRAV11	TF binding region
TRAV9-1	TF binding region
TRAV12-1	TF binding region
TRAV12-2	TF binding region
TRAV8-3	TF binding region
TRAV8-2	CpG island
TRAV6	CpG island
TRAV8-1	CpG island
ENSG00000222776	CpG island
TRAV13-1	CpG island
TRAV7	CpG island
TRAV10	CpG island
TRAV11	CpG island
TRAV9-1	CpG island
TRAV12-1	CpG island
TRAV12-2	CpG island
TRAV8-3	CpG island
ENSG00000211784	chromatin interactions
ENSG00000211779	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000256379	chromatin interactions

Extended variants
information (count: 3137 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3137 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4982501	chr14:22229021-22229022	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4982502	chr14:22229052-22229053	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4982503	chr14:22229079-22229080	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113492389	chr14:22229098-22229099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139160838	chr14:22229153-22229154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4982504	chr14:22229184-22229185	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs565068515	chr14:22232443-22232444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs548842374	chr14:22232459-22232460	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs369199986	chr14:22232468-22232469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs12435882	chr14:22232479-22232480	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs113782163	chr14:22232484-22232485	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547594059	chr14:22232537-22232538	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs189780001	chr14:22232583-22232584	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542164781	chr14:22235620-22235621	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11157210	chr14:22235659-22235660	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs28449295	chr14:22235672-22235673	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11157211	chr14:22235722-22235723	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs375003672	chr14:22235730-22235731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528737919	chr14:22235740-22235741	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528295669	chr14:22235746-22235747	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557559769	chr14:22235995-22235996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs577678464	chr14:22236002-22236003	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34929219	chr14:22236004-22236005	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs556940569	chr14:22236007-22236008	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs139683165	chr14:22236016-22236017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12587357	chr14:22236031-22236032	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12587521	chr14:22236047-22236048	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528259455	chr14:22236057-22236058	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs544810897	chr14:22236074-22236075	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs538986650	chr14:22236076-22236077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs555373527	chr14:22236096-22236097	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs17182782	chr14:22236105-22236106	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs531055952	chr14:22236132-22236133	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550665782	chr14:22236203-22236204	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs74836476	chr14:22236214-22236215	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35978792	chr14:22236218-22236219	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs547310977	chr14:22236238-22236239	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567212639	chr14:22236276-22236277	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11623274	chr14:22236316-22236317	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs34258387	chr14:22236370-22236371	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35342879	chr14:22236374-22236375	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs537168652	chr14:22236444-22236445	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs78257126	chr14:22236459-22236460	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs760007	chr14:22236469-22236470	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542252850	chr14:22236486-22236487	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552806017	chr14:22236493-22236494	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572803687	chr14:22236525-22236526	Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs150070238	chr14:22236538-22236539	Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535593050	chr14:22236570-22236571	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530652004	chr14:22236583-22236584	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21364760	CNVD
Autism	22102821	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lysinuric protein intolerance	18716612	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22228600-22229200	Enhancers	H9 Cell Line	embryonic stem cell
2	chr14:22236200-22236800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr14:22236200-22237000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:22236200-22237400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr14:22236200-22237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:22236400-22236600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr14:22236400-22237000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr14:22236600-22236800	Enhancers	Primary T cells fromperipheralblood	blood
9	chr14:22236600-22237000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:22236600-22237000	Active TSS	Thymus	Thymus
11	chr14:22236600-22237400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:22236800-22237000	Enhancers	Fetal Thymus	thymus
13	chr14:22236800-22237200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr14:22236800-22237200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
15	chr14:22236800-22237400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:22236800-22237400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:22237000-22244600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr14:22237400-22239600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr14:22237400-22245000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:22239400-22240200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:22239600-22240200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr14:22239600-22240400	Enhancers	HMEC	breast
23	chr14:22239600-22240400	Enhancers	NHEK	skin
24	chr14:22239800-22240200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:22239800-22240400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr14:22240000-22244600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr14:22241400-22242000	Enhancers	HepG2	liver
28	chr14:22244400-22245400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr14:22244400-22245600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr14:22244600-22245400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr14:22244600-22245400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr14:22244800-22245600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr14:22245000-22245200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr14:22245200-22245800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:22245400-22248600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr14:22245400-22248600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr14:22245400-22248600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr14:22245800-22246200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:22246200-22246400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr14:22246400-22246800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:22248600-22248800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr14:22248600-22248800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr14:22248600-22248800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:22248600-22248800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr14:22248600-22249000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr14:22248800-22249000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:22248800-22249200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr14:22249000-22249200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:22249200-22250200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:22250000-22250200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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