Variant report

Variant	esv3321940
Chromosome Location	chr12:123319399-123321597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:733)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123320826-123321038	K562	blood:	n/a	n/a
2	ARID3A	chr12:123320755-123321036	HepG2	liver:	n/a	n/a
3	ATF1	chr12:123321174-123321429	K562	blood:	n/a	n/a
4	ATF2	chr12:123320995-123321471	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:123320768-123320774	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:123320030-123320402	GM12878	blood:	n/a	chr12:123320080-123320096
7	BHLHE40	chr12:123320002-123320176	K562	blood:	n/a	chr12:123320080-123320096
8	BHLHE40	chr12:123320693-123320914	K562	blood:	n/a	n/a
9	BHLHE40	chr12:123321126-123321428	K562	blood:	n/a	n/a
10	CCNT2	chr12:123319962-123320553	K562	blood:	n/a	n/a
11	CEBPB	chr12:123318900-123319567	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:123319242-123319454	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:123319251-123319505	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPD	chr12:123320309-123320573	HepG2	liver:	n/a	n/a
15	CHD2	chr12:123318948-123320148	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr12:123320920-123321091	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr12:123320972-123321333	GM12878	blood:	n/a	n/a
18	CREB1	chr12:123319927-123320161	A549	lung:	n/a	n/a
19	CTCF	chr12:123321200-123321350	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr12:123319280-123319430	NHEK	skin:	n/a	n/a
21	CTCF	chr12:123320300-123320450	Caco-2	colon:	n/a	n/a
22	CTCF	chr12:123320320-123320452	GM19239	blood:	n/a	n/a
23	CTCF	chr12:123320600-123320750	GM12865	blood:	n/a	n/a
24	CTCF	chr12:123320241-123320586	K562	blood:	n/a	n/a
25	CTCF	chr12:123320920-123321070	NB4	blood:	n/a	n/a
26	CTCF	chr12:123320300-123320450	SAEC	small airway:	n/a	n/a
27	CTCF	chr12:123320312-123320433	GM19240	blood:	n/a	n/a
28	CTCF	chr12:123320280-123320430	GM12867	blood:	n/a	n/a
29	CTCF	chr12:123320314-123320445	GM19238	blood:	n/a	n/a
30	CTCF	chr12:123319260-123319410	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr12:123319360-123319510	HEK293	kidney:	n/a	n/a
32	CTCF	chr12:123320260-123320410	GM12873	blood:	n/a	n/a
33	CTCF	chr12:123320332-123320440	GM13976	blood:	n/a	n/a
34	CTCF	chr12:123320242-123320451	K562	blood:	n/a	n/a
35	CTCF	chr12:123320180-123320330	AG04449	skin:	n/a	n/a
36	CTCF	chr12:123320347-123320482	GM10248	blood:	n/a	n/a
37	CTCF	chr12:123320260-123320410	GM12874	blood:	n/a	n/a
38	CTCF	chr12:123320334-123320429	GM12892	blood:	n/a	n/a
39	CTCF	chr12:123320319-123320436	GM13977	blood:	n/a	n/a
40	CTCF	chr12:123321520-123321670	NB4	blood:	n/a	n/a
41	CTCF	chr12:123320366-123320430	GM20000	blood:	n/a	n/a
42	CTCF	chr12:123320260-123320410	GM12871	blood:	n/a	n/a
43	CTCF	chr12:123320321-123320466	GM10266	blood:	n/a	n/a
44	CTCF	chr12:123319280-123319430	HRE	kidney:	n/a	n/a
45	CTCF	chr12:123319320-123319470	GM12874	blood:	n/a	n/a
46	CTCF	chr12:123320230-123320545	GM12878	blood:	n/a	n/a
47	CTCF	chr12:123320260-123320410	HMEC	breast:	n/a	n/a
48	CUX1	chr12:123321475-123321740	GM12878	blood:	n/a	n/a
49	E2F4	chr12:123320870-123320978	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr12:123319913-123320183	K562	blood:	n/a	chr12:123320087-123320097 chr12:123320084-123320094

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123321254-123321304	AG09319	gingival:	n/a
2	chr12:123321254-123321304	AG09319	gingival:	n/a
3	chr12:123320057-123320107	Jurkat	blood:	n/a
4	chr12:123321254-123321304	HCPEpiC	choroid plexus:	n/a
5	chr12:123319900-123319950	HIPEpiC	eye:	n/a
6	chr12:123319906-123319956	HCM	heart:	n/a
7	chr12:123319906-123319956	ProgFib	skin:	n/a
8	chr12:123319900-123319950	NT2-D1	testis:	n/a
9	chr12:123319981-123320031	HCM	heart:	n/a
10	chr12:123320611-123320661	U87	brain:	n/a
11	chr12:123319906-123319956	HEEpiC	esophagus:	n/a
12	chr12:123319906-123319956	SKMC	muscle:	n/a
13	chr12:123320915-123320965	SK-N-MC	brain:	n/a
14	chr12:123321254-123321304	RPTEC	kidney:	n/a
15	chr12:123320057-123320107	HIPEpiC	eye:	n/a
16	chr12:123319906-123319956	AG04449	skin:	fetal
17	chr12:123319894-123319944	HCT-116	colon:	n/a
18	chr12:123320057-123320107	HCM	heart:	n/a
19	chr12:123320751-123320801	SK-N-SH	brain:	n/a
20	chr12:123320751-123320801	HEK293	kidney:	embryo
21	chr12:123321307-123321357	T-47D	breast:	n/a
22	chr12:123320751-123320801	NHBE	bronchial:	n/a
23	chr12:123321307-123321357	MCF10A-Er-Src	breast:	n/a
24	chr12:123320057-123320107	PFSK-1	brain:	n/a
25	chr12:123321254-123321304	BJ	skin:	n/a
26	chr12:123319894-123319944	HCF	heart:	n/a
27	chr12:123319900-123319950	Jurkat	blood:	n/a
28	chr12:123320751-123320801	GM06990	blood:	n/a
29	chr12:123319894-123319944	HNPCEpiC	eye:	n/a
30	chr12:123320751-123320801	PANC-1	pancreas:	n/a
31	chr12:123320915-123320965	GM19239	blood:	n/a
32	chr12:123321254-123321304	T-47D	breast:	n/a
33	chr12:123320611-123320661	SK-N-SH_RA	brain:	n/a
34	chr12:123319366-123319416	Hepatocyte	liver:	n/a
35	chr12:123321334-123321384	GM12891	blood:	n/a
36	chr12:123319894-123319944	NB4	blood:	n/a
37	chr12:123320611-123320661	CMK	blood:	n/a
38	chr12:123321334-123321384	Jurkat	blood:	n/a
39	chr12:123319906-123319956	GM12878	blood:	n/a
40	chr12:123320057-123320107	A549	lung:	n/a
41	chr12:123320611-123320661	SK-N-SH	brain:	n/a
42	chr12:123321307-123321357	U87	brain:	n/a
43	chr12:123320611-123320661	GM12892	blood:	n/a
44	chr12:123319981-123320031	SKMC	muscle:	n/a
45	chr12:123319981-123320031	HEK293	kidney:	embryo
46	chr12:123320751-123320801	HNPCEpiC	eye:	n/a
47	chr12:123319900-123319950	BE2_C	brain:	n/a
48	chr12:123321254-123321304	GM06990	blood:	n/a
49	chr12:123321334-123321384	H1-hESC	embryonic stem cell:	embryo
50	chr12:123319981-123320031	RPTEC	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123318920..123320804-chr12:123431971..123434703,2	MCF-7	breast:
2	chr12:123321572..123324516-chr12:123371831..123374446,2	MCF-7	breast:
3	chr12:123317692..123320507-chr12:123463597..123466562,3	MCF-7	breast:
4	chr12:123317720..123322313-chr12:123372173..123377754,7	MCF-7	breast:
5	chr12:123321295..123323539-chr12:123344367..123346467,3	MCF-7	breast:
6	chr12:123320203..123322846-chr12:123716653..123718204,2	MCF-7	breast:
7	chr12:123237061..123238610-chr12:123318389..123320839,2	MCF-7	breast:
8	chr12:123319262..123321924-chr12:123450152..123453465,3	K562	blood:
9	chr12:123321243..123322853-chr12:123379142..123381791,2	MCF-7	breast:
10	chr12:123318894..123320705-chr12:123342894..123344549,3	MCF-7	breast:
11	chr12:123319497..123321053-chr12:123333768..123335476,2	K562	blood:
12	chr12:123319192..123322007-chr12:123336993..123339222,2	MCF-7	breast:
13	chr12:123318351..123322726-chr12:123344658..123350717,8	MCF-7	breast:
14	chr12:123319135..123321319-chr3:160936978..160939441,2	MCF-7	breast:
15	chr12:123257747..123262116-chr12:123318149..123321331,4	MCF-7	breast:
16	chr12:123213106..123215069-chr12:123321149..123322935,2	MCF-7	breast:
17	chr12:123321334..123323006-chr12:123430937..123432965,2	MCF-7	breast:
18	chr12:123318760..123321217-chr12:123449684..123452450,2	K562	blood:
19	chr12:123321291..123323892-chr12:123444965..123447071,2	MCF-7	breast:
20	chr12:123318837..123320791-chr12:123463752..123466824,3	MCF-7	breast:
21	chr12:123318440..123320805-chr12:123633475..123636263,2	MCF-7	breast:
22	chr12:123320093..123322586-chr12:123715495..123717565,2	K562	blood:
23	chr12:123318632..123320877-chr12:123355595..123357643,2	MCF-7	breast:

No data

Variant related genes	Relation type
HIP1R	TF binding region
HIP1R	CpG island
ENSG00000130783	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000169251	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000090975	chromatin interactions
ENSG00000139722	chromatin interactions
ENSG00000139726	chromatin interactions
ENSG00000182196	chromatin interactions
ENSG00000150967	chromatin interactions
ENSG00000130787	chromatin interactions
ENSG00000256152	chromatin interactions

Extended variants
information (count: 47 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:47 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570055350	chr12:123319444-123319445	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs370652215	chr12:123319464-123319465	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs548968897	chr12:123319475-123319476	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs567626038	chr12:123319565-123319566	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs535102258	chr12:123319604-123319605	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs112066678	chr12:123319647-123319648	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs572201084	chr12:123319695-123319696	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs539684752	chr12:123319708-123319709	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs191558208	chr12:123319772-123319773	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs576405428	chr12:123319817-123319818	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs540174077	chr12:123319880-123319881	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs376073613	chr12:123320070-123320071	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs368388843	chr12:123320076-123320077	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs371920695	chr12:123320086-123320087	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs545043313	chr12:123320195-123320196	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs561736715	chr12:123320551-123320552	Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs12820345	chr12:123320579-123320580	Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541101148	chr12:123320606-123320607	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs143280537	chr12:123320645-123320646	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs184035869	chr12:123320657-123320658	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs188112380	chr12:123320705-123320706	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs563593333	chr12:123320786-123320787	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs531132375	chr12:123320807-123320808	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs79355888	chr12:123320874-123320875	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs567630260	chr12:123320886-123320887	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs372781828	chr12:123320888-123320889	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs151280899	chr12:123320947-123320948	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs549732934	chr12:123320977-123320978	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs386767137	chr12:123320982-123320983	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs75691486	chr12:123320983-123320984	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs374073601	chr12:123321006-123321007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs193064287	chr12:123321018-123321019	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs547365557	chr12:123321051-123321052	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs566010988	chr12:123321053-123321054	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs79865695	chr12:123321066-123321067	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs377085616	chr12:123321085-123321086	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs141744568	chr12:123321165-123321166	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs147604211	chr12:123321259-123321260	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs569929258	chr12:123321268-123321269	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs367678990	chr12:123321381-123321382	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs75762911	chr12:123321405-123321406	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs555405034	chr12:123321445-123321446	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs573580627	chr12:123321461-123321462	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs540713889	chr12:123321487-123321488	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs12314544	chr12:123321497-123321498	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577323961	chr12:123321575-123321576	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs185353277	chr12:123321588-123321589	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123318800-123319400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
2	chr12:123318800-123319600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:123318800-123319600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr12:123318800-123319600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:123318800-123319600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:123318800-123319600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:123318800-123319600	Flanking Active TSS	Fetal Brain Male	brain
8	chr12:123318800-123319600	Flanking Active TSS	Fetal Heart	heart
9	chr12:123318800-123319600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr12:123318800-123319600	Flanking Active TSS	Hela-S3	cervix
11	chr12:123318800-123319600	Flanking Active TSS	HSMMtube	muscle
12	chr12:123318800-123319600	Flanking Active TSS	HUVEC	blood vessel
13	chr12:123318800-123319600	Flanking Active TSS	NHLF	lung
14	chr12:123318800-123319800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr12:123318800-123319800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:123318800-123319800	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr12:123318800-123319800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:123318800-123319800	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr12:123318800-123319800	Flanking Active TSS	HMEC	breast
20	chr12:123318800-123320600	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr12:123318800-123320600	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr12:123318800-123320600	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr12:123318800-123321000	Active TSS	Brain Cingulate Gyrus	brain
24	chr12:123318800-123321200	Active TSS	H9 Cell Line	embryonic stem cell
25	chr12:123318800-123321200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:123318800-123321600	Active TSS	Brain Hippocampus Middle	brain
27	chr12:123318800-123321600	Active TSS	Ovary	ovary
28	chr12:123318800-123321600	Active TSS	Stomach Smooth Muscle	stomach
29	chr12:123318800-123322400	Active TSS	Brain Angular Gyrus	brain
30	chr12:123318800-123322400	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr12:123319000-123319400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:123319000-123319400	Enhancers	Spleen	Spleen
33	chr12:123319000-123319600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:123319000-123319600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr12:123319000-123319600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:123319000-123319600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:123319000-123319600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr12:123319000-123319600	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr12:123319000-123319600	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
40	chr12:123319000-123319600	Flanking Active TSS	Pancreas	Pancrea
41	chr12:123319000-123319600	Flanking Active TSS	Rectal Smooth Muscle	rectum
42	chr12:123319000-123319600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr12:123319000-123319600	Flanking Active TSS	HSMM	muscle
44	chr12:123319000-123319600	Flanking Active TSS	NH-A	brain
45	chr12:123319000-123319600	Flanking Active TSS	NHEK	skin
46	chr12:123319000-123319800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr12:123319000-123319800	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr12:123319000-123319800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
49	chr12:123319000-123319800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr12:123319000-123319800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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