Variant report

Variant	rs11253521
Chromosome Location	chr10:976416-976417
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr10:976393-977067	MCF-7	breast:	n/a	n/a
2	EBF1	chr10:975918-976854	GM12878	blood:	n/a	n/a
3	PML	chr10:976099-976774	GM12878	blood:	n/a	chr10:976583-976591
4	MAZ	chr10:976393-976889	K562	blood:	n/a	n/a
5	GABPA	chr10:976248-977099	MCF-7	breast:	n/a	chr10:976865-976874
6	MAZ	chr10:976375-978384	IMR90	lung:	n/a	chr10:978023-978030
7	HCFC1	chr10:976026-976742	K562	blood:	n/a	n/a
8	MAX	chr10:976363-976936	K562	blood:	n/a	n/a
9	POLR2A	chr10:976372-976704	GM12892	blood:	n/a	n/a
10	POLR2A	chr10:976006-978240	IMR90	lung:	n/a	n/a
11	POLR2A	chr10:975961-978259	GM18526	blood:	n/a	n/a
12	TBP	chr10:975879-976632	GM12878	blood:	n/a	n/a
13	POLR2A	chr10:975533-977115	K562	blood:	n/a	n/a
14	POLR2A	chr10:975992-978265	GM12892	blood:	n/a	n/a
15	UBTF	chr10:975941-977823	K562	blood:	n/a	n/a
16	NR2F2	chr10:976325-977290	MCF-7	breast:	n/a	n/a
17	TBL1XR1	chr10:975833-976782	GM12878	blood:	n/a	n/a
18	RELA	chr10:975973-976541	GM19099	blood:	n/a	n/a
19	HEY1	chr10:976332-977101	K562	blood:	n/a	chr10:976783-976798 chr10:976864-976879
20	POLR2A	chr10:975853-977885	GM12892	blood:	n/a	n/a
21	GATA3	chr10:976400-976959	T-47D	breast:	n/a	n/a
22	UBTF	chr10:976383-977244	K562	blood:	n/a	n/a
23	JUND	chr10:976066-976832	K562	blood:	n/a	chr10:976780-976789
24	POLR2A	chr10:975884-976854	GM12891	blood:	n/a	n/a
25	POLR2A	chr10:976177-976841	GM12891	blood:	n/a	n/a
26	POLR2A	chr10:975803-976893	GM12878	blood:	n/a	n/a
27	MXI1	chr10:975345-978313	SK-N-SH	brain:	n/a	chr10:976045-976054
28	POLR2A	chr10:976181-977220	H1-hESC	embryonic stem cell:	n/a	n/a
29	MXI1	chr10:976261-976723	K562	blood:	n/a	n/a
30	POLR2A	chr10:975829-976805	GM12891	blood:	n/a	n/a
31	POLR2A	chr10:975955-978318	GM19193	blood:	n/a	n/a
32	MAZ	chr10:976008-976416	GM12878	blood:	n/a	n/a
33	SIN3A	chr10:976300-977999	H1-hESC	embryonic stem cell:	n/a	chr10:977346-977359 chr10:977808-977819 chr10:977738-977749
34	BCLAF1	chr10:976320-976797	GM12878	blood:	n/a	n/a
35	POLR2A	chr10:975784-976804	GM12878	blood:	n/a	n/a
36	NFE2	chr10:976389-976434	GM12878	blood:	n/a	n/a
37	CHD1	chr10:975406-978308	IMR90	lung:	n/a	chr10:977804-977814 chr10:977690-977700
38	POLR2A	chr10:976340-977817	Hela-S3	cervix:	n/a	n/a
39	RUNX3	chr10:975820-976698	GM12878	blood:	n/a	n/a
40	POLR2A	chr10:975972-977091	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr10:976020-976713	GM12878	blood:	n/a	n/a
42	SIN3AK20	chr10:976319-976923	K562	blood:	n/a	n/a
43	STAT5A	chr10:975873-976689	GM12878	blood:	n/a	n/a
44	POLR2A	chr10:976326-976435	K562	blood:	n/a	n/a
45	POLR2A	chr10:975819-977213	GM12878	blood:	n/a	n/a
46	POLR2A	chr10:976414-978268	Raji	blood:	n/a	n/a
47	ELF1	chr10:976320-977060	MCF-7	breast:	n/a	chr10:976737-976750 chr10:976738-976749
48	USF2	chr10:975878-976444	GM12878	blood:	n/a	n/a
49	MAFF	chr10:975865-976575	K562	blood:	n/a	n/a
50	ELF1	chr10:976379-977297	MCF-7	breast:	n/a	chr10:976737-976750 chr10:976738-976749

No.	Distal block	Cell Line	Cell type
1	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
2	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
3	chr10:974758..977274-chr10:1018618..1021450,2	K562	blood:
4	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
5	chr10:975309..980832-chr10:1031626..1035973,12	K562	blood:
6	chr10:975582..978698-chr10:1119494..1122267,3	MCF-7	breast:
7	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
8	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
9	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
10	chr10:974758..976966-chr10:1110782..1112393,2	MCF-7	breast:
11	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
12	chr10:974636..980819-chr10:1029938..1037009,15	MCF-7	breast:
13	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000229869	TF binding region
ENSG00000238924	Chromatin interaction
ENSG00000067064	Chromatin interaction
ENSG00000205740	Chromatin interaction
ENSG00000107937	Chromatin interaction
ENSG00000047056	Chromatin interaction

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs1013505	0.90[CEU][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10508208	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs10904577	1.00[ASN][1000 genomes]
rs10904580	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10904581	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10904583	1.00[CEU][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10904584	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1106064	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253444	0.89[CEU][hapmap]
rs11253445	0.90[CEU][hapmap]
rs11253446	0.90[CEU][hapmap]
rs11253458	0.94[CEU][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs11253459	0.88[CEU][hapmap]
rs11253460	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253465	1.00[ASN][1000 genomes]
rs11253467	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253468	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253473	1.00[ASN][1000 genomes]
rs11253475	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253485	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253488	0.93[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253492	0.95[CEU][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs11253493	0.95[CEU][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs11253494	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs11253495	0.94[CEU][hapmap];0.85[YRI][hapmap]
rs11253499	1.00[ASN][1000 genomes]
rs11253504	0.88[CEU][hapmap]
rs11253509	1.00[CEU][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253511	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253513	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253517	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253520	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11812170	1.00[ASN][1000 genomes]
rs11812523	1.00[ASN][1000 genomes]
rs11813210	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs11815185	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11816064	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs11817793	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs11818288	1.00[ASN][1000 genomes]
rs11818325	1.00[ASN][1000 genomes]
rs12240651	1.00[ASN][1000 genomes]
rs12244253	1.00[ASN][1000 genomes]
rs12244355	1.00[ASN][1000 genomes]
rs12249634	1.00[ASN][1000 genomes]
rs12249828	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs12250936	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs12250937	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs12251396	1.00[ASN][1000 genomes]
rs12254002	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs12258388	1.00[ASN][1000 genomes]
rs12259338	1.00[CEU][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12259720	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12259801	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260800	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs12261911	1.00[ASN][1000 genomes]
rs12264390	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12264711	1.00[ASN][1000 genomes]
rs12267709	1.00[ASN][1000 genomes]
rs12354639	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12357633	0.90[CEU][hapmap]
rs12359645	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12360270	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12761424	1.00[CEU][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12762973	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12763396	0.94[CEU][hapmap];0.85[YRI][hapmap];1.00[ASN][1000 genomes]
rs12764024	0.84[CEU][hapmap];1.00[ASN][1000 genomes]
rs12765174	1.00[ASN][1000 genomes]
rs12766381	1.00[ASN][1000 genomes]
rs12768348	0.90[CEU][hapmap]
rs12769002	0.89[CEU][hapmap]
rs12769431	1.00[ASN][1000 genomes]
rs12769873	0.95[CEU][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs12770190	0.89[CEU][hapmap];1.00[ASN][1000 genomes]
rs12774985	0.90[CEU][hapmap]
rs12778891	1.00[ASN][1000 genomes]
rs12783472	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13377166	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs1341741	0.94[CEU][hapmap]
rs1341742	1.00[ASN][1000 genomes]
rs1539174	1.00[CEU][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1555899	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs17159950	0.93[CEU][hapmap];1.00[ASN][1000 genomes]
rs17159970	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs2050944	0.90[CEU][hapmap];1.00[ASN][1000 genomes]
rs34254874	1.00[ASN][1000 genomes]
rs34270014	1.00[ASN][1000 genomes]
rs34284130	1.00[ASN][1000 genomes]
rs34405399	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34433840	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34847097	1.00[ASN][1000 genomes]
rs35174953	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35394603	1.00[ASN][1000 genomes]
rs35567307	1.00[ASN][1000 genomes]
rs35637113	1.00[ASN][1000 genomes]
rs35693858	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35825568	1.00[ASN][1000 genomes]
rs35968821	1.00[ASN][1000 genomes]
rs4522091	0.95[CEU][hapmap];0.83[YRI][hapmap];1.00[ASN][1000 genomes]
rs56318703	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56347655	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61830929	1.00[ASN][1000 genomes]
rs61830932	1.00[ASN][1000 genomes]
rs7067865	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs7074642	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs7077278	0.94[CEU][hapmap];1.00[ASN][1000 genomes]
rs72778229	1.00[ASN][1000 genomes]
rs765867	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs7908138	1.00[CEU][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7914758	0.90[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv1043812	chr10:776547-981126	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv540406	chr10:776547-981126	Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv948978	chr10:813426-1019115	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
12	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
13	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
14	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
15	nsv825207	chr10:957020-1005451	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
17	nsv825208	chr10:965883-1004836	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
18	esv3381643	chr10:975752-979950	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	esv3422446	chr10:975977-978525	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	esv3394984	chr10:976102-979400	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	esv3422999	chr10:976377-979825	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:974600-976600	Weak transcription	Spleen	Spleen
2	chr10:974600-976800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:975200-976600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr10:975200-976600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:975200-976600	Transcr. at gene 5' and 3'	K562	blood
6	chr10:975200-979200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:975400-976600	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr10:975400-976600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:975400-976800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:975400-976800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr10:975600-976600	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr10:975600-976600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:975600-976600	Flanking Active TSS	Dnd41	blood
14	chr10:975600-976600	Flanking Active TSS	HMEC	breast
15	chr10:975600-976600	Flanking Active TSS	HUVEC	blood vessel
16	chr10:975600-976600	Flanking Active TSS	Osteobl	bone
17	chr10:975600-978400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr10:975600-978400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:975600-978400	Active TSS	GM12878-XiMat	blood
20	chr10:975600-978800	Active TSS	Psoas Muscle	Psoas
21	chr10:975600-979000	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr10:975800-976600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr10:975800-976600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr10:975800-976600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr10:975800-976600	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr10:975800-976600	Flanking Active TSS	Liver	Liver
27	chr10:975800-976600	Flanking Active TSS	Fetal Brain Female	brain
28	chr10:975800-976600	Flanking Active TSS	Fetal Thymus	thymus
29	chr10:975800-976800	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr10:975800-977200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:975800-978200	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr10:975800-978200	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr10:975800-978200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:975800-978400	Active TSS	H9 Cell Line	embryonic stem cell
35	chr10:975800-978400	Active TSS	Fetal Intestine Large	intestine
36	chr10:975800-978400	Active TSS	NHLF	lung
37	chr10:976000-976600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr10:976000-976600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr10:976000-976600	Flanking Active TSS	Brain Angular Gyrus	brain
40	chr10:976000-976600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:976000-976600	Flanking Active TSS	Fetal Lung	lung
42	chr10:976000-976600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr10:976000-976800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr10:976000-976800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr10:976000-976800	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr10:976000-976800	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr10:976000-976800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr10:976000-976800	Flanking Active TSS	Fetal Brain Male	brain
49	chr10:976000-976800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr10:976000-977200	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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