Variant report

Variant	esv1817413
Chromosome Location	chr12:1625937-1640595
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	chr12:1628548-1628571	HepG2	liver:	n/a	n/a
2	BACH1	chr12:1640441-1640668	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:1632875-1633009	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr12:1628282-1628867	A549	lung:	n/a	chr12:1628532-1628541
5	BCL3	chr12:1628296-1628851	A549	lung:	n/a	chr12:1628532-1628541
6	BHLHE40	chr12:1635197-1635315	K562	blood:	n/a	n/a
7	BHLHE40	chr12:1639049-1639239	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:1635096-1635410	GM12878	blood:	n/a	n/a
9	CCNT2	chr12:1639395-1639806	K562	blood:	n/a	n/a
10	CCNT2	chr12:1640162-1640764	K562	blood:	n/a	chr12:1640439-1640448
11	CEBPB	chr12:1628415-1628821	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:1625949-1626001	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:1625793-1626078	K562	blood:	n/a	n/a
14	CEBPB	chr12:1625807-1626388	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:1633008-1633195	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr12:1640471-1640598	GM12878	blood:	n/a	n/a
17	CHD1	chr12:1639146-1639271	GM12878	blood:	n/a	n/a
18	CHD2	chr12:1632843-1633160	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr12:1628341-1628701	A549	lung:	n/a	n/a
20	CTCF	chr12:1626387-1626558	MCF-7	breast:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
21	CTCF	chr12:1640480-1640630	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr12:1626380-1626530	MCF-7	breast:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
23	CTCF	chr12:1626388-1626571	GM13976	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
24	CTCF	chr12:1626380-1626530	HUVEC	blood vessel:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
25	CTCF	chr12:1626420-1626570	HMF	breast:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
26	CTCF	chr12:1626436-1626525	Lung_OC	lung:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
27	CTCF	chr12:1626440-1626590	HAc	cerebellar:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
28	CTCF	chr12:1626380-1626530	WI-38	lung:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
29	CTCF	chr12:1626382-1626599	Medullo	brain:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
30	CTCF	chr12:1626340-1626490	HCM	heart:	n/a	chr12:1626481-1626490
31	CTCF	chr12:1626340-1626490	AG04449	skin:	n/a	chr12:1626481-1626490
32	CTCF	chr12:1626460-1626610	HCM	heart:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
33	CTCF	chr12:1626400-1626550	HCFaa	heart:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
34	CTCF	chr12:1626264-1626683	H1-hESC	embryonic stem cell:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
35	CTCF	chr12:1626248-1626711	H1-hESC	embryonic stem cell:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
36	CTCF	chr12:1626440-1626590	AG04450	lung:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
37	CTCF	chr12:1626440-1626590	GM12868	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
38	CTCF	chr12:1626320-1626470	A549	lung:	n/a	n/a
39	CTCF	chr12:1626304-1626646	IMR90	lung:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
40	CTCF	chr12:1626361-1626585	GM20000	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
41	CTCF	chr12:1626380-1626530	NHEK	skin:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
42	CTCF	chr12:1626340-1626490	HL-60	blood:	n/a	chr12:1626481-1626490
43	CTCF	chr12:1626385-1626555	Gliobla	brain:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
44	CTCF	chr12:1626360-1626510	GM06990	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
45	CTCF	chr12:1626400-1626550	GM12871	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
46	CTCF	chr12:1626780-1626930	GM12868	blood:	n/a	n/a
47	CTCF	chr12:1626420-1626570	HPAF	blood vessel:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
48	CTCF	chr12:1626420-1626570	GM12865	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
49	CTCF	chr12:1626420-1626570	HEK293	kidney:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494
50	CTCF	chr12:1626380-1626530	GM12866	blood:	n/a	chr12:1626480-1626501 chr12:1626478-1626496 chr12:1626481-1626490 chr12:1626479-1626495 chr12:1626481-1626494

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1639527-1639577	LNCaP	prostate:	n/a
2	chr12:1633258-1633308	NH-A	brain:	n/a
3	chr12:1633258-1633308	HRE	kidney:	n/a
4	chr12:1628620-1628670	PFSK-1	brain:	n/a
5	chr12:1639527-1639577	PANC-1	pancreas:	n/a
6	chr12:1639527-1639577	RPTEC	kidney:	n/a
7	chr12:1640392-1640442	Hela-S3	cervix:	n/a
8	chr12:1635982-1636032	HUVEC	blood vessel:	n/a
9	chr12:1628620-1628670	SAEC	small airway:	n/a
10	chr12:1637124-1637174	GM06990	blood:	n/a
11	chr12:1639534-1639584	SK-N-SH	brain:	n/a
12	chr12:1637124-1637174	NB4	blood:	n/a
13	chr12:1639034-1639084	MCF-7	breast:	n/a
14	chr12:1639034-1639084	NH-A	brain:	n/a
15	chr12:1639534-1639584	ProgFib	skin:	n/a
16	chr12:1637124-1637174	SK-N-SH_RA	brain:	n/a
17	chr12:1639534-1639584	HCM	heart:	n/a
18	chr12:1628620-1628670	BJ	skin:	n/a
19	chr12:1639534-1639584	Jurkat	blood:	n/a
20	chr12:1635982-1636032	CMK	blood:	n/a
21	chr12:1628620-1628670	GM12892	blood:	n/a
22	chr12:1639034-1639084	HCF	heart:	n/a
23	chr12:1640392-1640442	HNPCEpiC	eye:	n/a
24	chr12:1640392-1640442	IMR90	lung:	fetal
25	chr12:1639534-1639584	SK-N-MC	brain:	n/a
26	chr12:1633258-1633308	IMR90	lung:	fetal
27	chr12:1633258-1633308	SKMC	muscle:	n/a
28	chr12:1639534-1639584	GM12878	blood:	n/a
29	chr12:1640392-1640442	HepG2	liver:	n/a
30	chr12:1639034-1639084	RPTEC	kidney:	n/a
31	chr12:1635982-1636032	SAEC	small airway:	n/a
32	chr12:1639534-1639584	ovcar-3	ovarian:	n/a
33	chr12:1639534-1639584	MCF10A-Er-Src	breast:	n/a
34	chr12:1640392-1640442	RPTEC	kidney:	n/a
35	chr12:1628620-1628670	NT2-D1	testis:	n/a
36	chr12:1639527-1639577	A549	lung:	n/a
37	chr12:1639527-1639577	NHBE	bronchial:	n/a
38	chr12:1639527-1639577	SK-N-SH_RA	brain:	n/a
39	chr12:1628620-1628670	HRCEpiC	kidney:	n/a
40	chr12:1639527-1639577	HCF	heart:	n/a
41	chr12:1639534-1639584	NHBE	bronchial:	n/a
42	chr12:1640392-1640442	U87	brain:	n/a
43	chr12:1635982-1636032	BJ	skin:	n/a
44	chr12:1639034-1639084	AG10803	skin:	n/a
45	chr12:1635982-1636032	HNPCEpiC	eye:	n/a
46	chr12:1640392-1640442	HIPEpiC	eye:	n/a
47	chr12:1633258-1633308	AG04449	skin:	fetal
48	chr12:1640392-1640442	PrEC	prostate:	n/a
49	chr12:1635982-1636032	T-47D	breast:	n/a
50	chr12:1639527-1639577	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1630597..1633129-chr12:1648512..1650359,2	MCF-7	breast:
2	chr12:1608089..1610158-chr12:1624609..1627312,2	K562	blood:
3	chr12:1631412..1633755-chr12:1644616..1647066,2	K562	blood:
4	chr12:1615017..1617424-chr12:1628113..1630003,2	MCF-7	breast:
5	chr12:1626725..1629627-chr12:1683737..1685681,2	MCF-7	breast:
6	chr12:1627927..1631783-chr12:1637016..1640816,5	K562	blood:
7	chr12:1626921..1630129-chr12:1639679..1644833,6	MCF-7	breast:
8	chr12:1635757..1638197-chr12:1659223..1662121,2	K562	blood:
9	chr12:1611483..1613501-chr12:1625253..1627123,2	K562	blood:
10	chr12:1629697..1630429-chr15:40937161..40938110,2	MCF-7	breast:
11	chr12:1226666..1228780-chr12:1626005..1628648,2	MCF-7	breast:
12	chr12:1632492..1634804-chr12:1681933..1684752,2	K562	blood:
13	chr12:1626153..1629399-chr12:1683454..1686746,3	MCF-7	breast:
14	chr12:1627443..1629034-chr12:1702544..1704207,2	MCF-7	breast:
15	chr12:1626245..1629061-chr12:1642130..1644083,2	MCF-7	breast:
16	chr12:1627927..1629732-chr12:1638277..1639813,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL14-4	chr12:1634111-1634529	l_580_chr12:1634110-1648432_liver

Variant related genes	Relation type
WNT5B	TF binding region
WNT5B	CpG island
ENSG00000171823	chromatin interactions
ENSG00000249628	chromatin interactions
ENSG00000111186	chromatin interactions

Extended variants
information (count: 676 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2189670	chr12:1625937-1625938	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114471106	chr12:1625959-1625960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567584447	chr12:1625992-1625993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185893237	chr12:1626011-1626012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188796580	chr12:1626014-1626015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374555738	chr12:1626039-1626040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34804863	chr12:1626043-1626044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561846628	chr12:1626063-1626064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527993144	chr12:1626141-1626142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534989586	chr12:1626157-1626158	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181346286	chr12:1626175-1626176	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186419779	chr12:1626180-1626181	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141893345	chr12:1626192-1626193	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568925494	chr12:1626217-1626218	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190923922	chr12:1626233-1626234	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372904790	chr12:1626244-1626245	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551373468	chr12:1626285-1626286	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566446737	chr12:1626307-1626308	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533784553	chr12:1626325-1626326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553586945	chr12:1626402-1626403	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10848505	chr12:1626412-1626413	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs536043037	chr12:1626413-1626414	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182821808	chr12:1626419-1626420	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575315716	chr12:1626432-1626433	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73044907	chr12:1626441-1626442	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557849226	chr12:1626442-1626443	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111332528	chr12:1626465-1626466	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557132931	chr12:1626521-1626522	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs540236649	chr12:1626535-1626536	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562013432	chr12:1626607-1626608	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529215098	chr12:1626613-1626614	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10848506	chr12:1626626-1626627	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs10773953	chr12:1626629-1626630	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533181695	chr12:1626630-1626631	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551461438	chr12:1626631-1626632	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561283628	chr12:1626751-1626752	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573310498	chr12:1626781-1626782	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566580921	chr12:1626785-1626786	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79434669	chr12:1626805-1626806	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12146724	chr12:1626838-1626839	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558687117	chr12:1626943-1626944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535804119	chr12:1626976-1626977	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557658541	chr12:1627011-1627012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569077420	chr12:1627030-1627031	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539656969	chr12:1627046-1627047	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs67719042	chr12:1627072-1627073	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573048275	chr12:1627144-1627145	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149765030	chr12:1627145-1627146	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532198792	chr12:1627170-1627171	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555513364	chr12:1627176-1627177	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1612200-1626000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr12:1614200-1626200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr12:1619000-1626000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:1619600-1626400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr12:1621400-1626000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:1624200-1626600	Weak transcription	HSMM	muscle
7	chr12:1625600-1626400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr12:1625800-1626400	Enhancers	NHEK	skin
9	chr12:1626000-1626400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:1626000-1626400	Enhancers	HMEC	breast
11	chr12:1626000-1626600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:1626000-1627400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:1626000-1628000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr12:1626000-1629400	Enhancers	NHDF-Ad	bronchial
15	chr12:1626200-1626400	Enhancers	Ovary	ovary
16	chr12:1626200-1626400	Enhancers	Osteobl	bone
17	chr12:1626200-1627200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:1626200-1627200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:1626200-1627800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:1626400-1626600	Flanking Active TSS	NHEK	skin
21	chr12:1626400-1626800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:1626400-1626800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:1626400-1626800	Flanking Active TSS	Osteobl	bone
24	chr12:1626400-1627000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:1626400-1627000	Enhancers	NH-A	brain
26	chr12:1626400-1627400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr12:1626400-1628000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:1626400-1629000	Flanking Active TSS	HMEC	breast
29	chr12:1626400-1629400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:1626400-1629400	Enhancers	NHLF	lung
31	chr12:1626600-1626800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr12:1626600-1626800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:1626600-1627400	Enhancers	HSMM	muscle
34	chr12:1626600-1627400	Enhancers	NHEK	skin
35	chr12:1626600-1627600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr12:1626600-1627800	Weak transcription	Ovary	ovary
37	chr12:1626600-1629000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr12:1626800-1627200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr12:1626800-1627600	Enhancers	Osteobl	bone
40	chr12:1626800-1628000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:1626800-1628400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:1627000-1627400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:1627000-1627400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr12:1627000-1627400	Weak transcription	NH-A	brain
45	chr12:1627000-1628200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr12:1627200-1627800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:1627200-1627800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:1627200-1628400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:1627200-1629200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:1627200-1629200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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