Variant report

Variant	rs2203197
Chromosome Location	chr10:5904918-5904919
allele	C/T
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	EBF1	chr10:5904188-5905055	GM12878	blood:	n/a	n/a
2	ATF2	chr10:5904094-5905203	GM12878	blood:	n/a	n/a
3	BATF	chr10:5904206-5904991	GM12878	blood:	n/a	n/a
4	RUNX3	chr10:5904062-5905077	GM12878	blood:	n/a	n/a
5	RELA	chr10:5904190-5905122	GM12891	blood:	n/a	n/a
6	MEF2C	chr10:5904074-5904934	GM12878	blood:	n/a	n/a
7	RELA	chr10:5904218-5905194	GM10847	blood:	n/a	n/a
8	USF2	chr10:5904390-5904991	GM12878	blood:	n/a	n/a
9	ZNF143	chr10:5904255-5905177	GM12878	blood:	n/a	n/a
10	CEBPB	chr10:5904056-5904980	GM12878	blood:	n/a	n/a
11	FOXM1	chr10:5904117-5904966	GM12878	blood:	n/a	n/a
12	NFIC	chr10:5903990-5904999	GM12878	blood:	n/a	n/a
13	BATF	chr10:5904143-5905100	GM12878	blood:	n/a	n/a
14	RELA	chr10:5904222-5905078	GM19099	blood:	n/a	n/a
15	RELA	chr10:5904198-5905142	GM18951	blood:	n/a	n/a
16	ELF1	chr10:5904152-5904932	GM12878	blood:	n/a	n/a
17	FOXM1	chr10:5904097-5905137	GM12878	blood:	n/a	n/a
18	STAT5A	chr10:5904140-5905167	GM12878	blood:	n/a	chr10:5904823-5904835 chr10:5904828-5904840
19	CTCF	chr10:5904483-5905254	GM12878	blood:	n/a	n/a
20	RUNX3	chr10:5904114-5905194	GM12878	blood:	n/a	n/a
21	RFX5	chr10:5904289-5904941	GM12878	blood:	n/a	n/a
22	EBF1	chr10:5904081-5905014	GM12878	blood:	n/a	n/a
23	MAX	chr10:5904303-5905159	GM12878	blood:	n/a	n/a
24	MTA3	chr10:5904091-5905002	GM12878	blood:	n/a	n/a
25	CREB1	chr10:5904117-5905044	GM12878	blood:	n/a	n/a
26	CREB1	chr10:5904075-5905144	GM12878	blood:	n/a	n/a
27	RELA	chr10:5904212-5905148	GM12892	blood:	n/a	n/a
28	IRF4	chr10:5904079-5905017	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:5904162-5905104	GM12878	blood:	n/a	n/a
30	JUND	chr10:5904109-5905287	GM12878	blood:	n/a	n/a
31	WRNIP1	chr10:5904206-5905242	GM12878	blood:	n/a	n/a
32	SP1	chr10:5904162-5905003	GM12878	blood:	n/a	n/a
33	RELA	chr10:5904235-5905187	GM15510	blood:	n/a	n/a
34	RCOR1	chr10:5904238-5904962	GM12878	blood:	n/a	n/a
35	CHD2	chr10:5904177-5905077	GM12878	blood:	n/a	n/a
36	NFIC	chr10:5904077-5905090	GM12878	blood:	n/a	n/a
37	TBL1XR1	chr10:5904174-5905087	GM12878	blood:	n/a	n/a
38	PAX5	chr10:5904126-5905042	GM12878	blood:	n/a	chr10:5904556-5904575
39	NFATC1	chr10:5904153-5905012	GM12878	blood:	n/a	n/a
40	RELA	chr10:5904257-5905126	GM19193	blood:	n/a	n/a
41	SMC3	chr10:5904239-5904999	GM12878	blood:	n/a	n/a
42	PAX5	chr10:5904143-5905041	GM12878	blood:	n/a	chr10:5904556-5904575
43	STAT3	chr10:5904209-5905028	GM12878	blood:	n/a	chr10:5904823-5904835 chr10:5904828-5904840
44	BCLAF1	chr10:5904038-5904983	GM12878	blood:	n/a	n/a
45	PAX5	chr10:5904088-5904982	GM12878	blood:	n/a	chr10:5904556-5904575
46	NFATC1	chr10:5904112-5904921	GM12878	blood:	n/a	n/a
47	RELA	chr10:5904180-5905070	GM18505	blood:	n/a	n/a
48	BCLAF1	chr10:5904086-5905107	GM12878	blood:	n/a	n/a
49	NRF1	chr10:5904230-5905006	GM12878	blood:	n/a	n/a
50	EP300	chr10:5904186-5905099	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
2	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
3	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000240180	TF binding region
ENSG00000272764	Chromatin interaction
ENSG00000134461	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000134452	Chromatin interaction

Extended variants
information (count: 95 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10795590	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10795591	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10795593	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10795595	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10795596	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10905299	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10905302	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10905303	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10905307	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10905316	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11255549	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255555	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255558	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11255564	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11255577	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11255581	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11524382	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12246906	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12246907	0.86[AMR][1000 genomes]
rs12250878	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12253826	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12255077	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12359234	0.89[TSI][hapmap];0.81[EUR][1000 genomes]
rs12774966	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.98[TSI][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12777477	0.81[EUR][1000 genomes]
rs12784539	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1512694	0.85[JPT][hapmap]
rs2104285	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2137423	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2203196	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2380200	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2380201	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2380205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2380208	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3954757	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4009521	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4256891	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4282894	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4282898	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4282899	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4287254	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4293038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4301704	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4330991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4421659	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4428973	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4468244	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4497300	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6602283	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6602284	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6602312	0.85[JPT][hapmap]
rs6602322	0.85[JPT][hapmap]
rs7072174	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.98[TSI][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7073128	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7098372	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7099029	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs713588	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7894083	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.98[TSI][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7894559	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7897260	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7898042	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7898059	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7901964	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7902205	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7903875	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7904512	0.82[JPT][hapmap]
rs7906635	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7907053	0.85[JPT][hapmap]
rs7907795	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7907914	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7908028	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7919044	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7919785	0.85[JPT][hapmap]
rs7923278	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7923781	0.82[JPT][hapmap]
rs867052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs907685	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907686	0.93[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.97[LWK][hapmap];0.87[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907688	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907689	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907690	0.81[EUR][1000 genomes]
rs9663697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9663995	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9732607	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats 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	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer 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
5	nsv5654	chr10:5868365-5930634	Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv825229	chr10:5886905-5967697	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv466722	chr10:5893268-5916201	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv549904	chr10:5893268-5916201	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv437655	chr10:5900973-5910361	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv520941	chr10:5903518-5904918	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv519773	chr10:5904300-5905231	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2203197	ANKRD16	cis	parietal	SCAN
rs2203197	ANKRD16	cis	cerebellum	SCAN

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5894600-5908600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:5894600-5908600	Weak transcription	K562	blood
3	chr10:5894600-5916800	Weak transcription	Spleen	Spleen
4	chr10:5896200-5912200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:5896400-5918200	Weak transcription	Fetal Lung	lung
6	chr10:5899800-5905000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr10:5900000-5916600	Weak transcription	Pancreas	Pancrea
8	chr10:5900400-5916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr10:5900600-5916200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr10:5900800-5910600	Weak transcription	Brain Germinal Matrix	brain
11	chr10:5901000-5916600	Weak transcription	Gastric	stomach
12	chr10:5901200-5918200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:5901400-5905000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr10:5901400-5915200	Weak transcription	Brain Hippocampus Middle	brain
15	chr10:5901600-5912600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr10:5901600-5915600	Weak transcription	Brain Anterior Caudate	brain
17	chr10:5901800-5910800	Weak transcription	Fetal Brain Female	brain
18	chr10:5902200-5905000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:5902200-5912600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr10:5902400-5905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr10:5902400-5908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:5902400-5918200	Weak transcription	Primary T cells from cord blood	blood
23	chr10:5902600-5910200	Weak transcription	Fetal Muscle Leg	muscle
24	chr10:5902800-5916200	Weak transcription	Fetal Intestine Large	intestine
25	chr10:5902800-5916600	Weak transcription	Brain Substantia Nigra	brain
26	chr10:5902800-5918000	Weak transcription	Lung	lung
27	chr10:5903000-5905200	Enhancers	HepG2	liver
28	chr10:5903000-5912400	Weak transcription	Fetal Heart	heart
29	chr10:5903000-5915400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr10:5903400-5911000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr10:5903400-5918200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr10:5903400-5925000	Weak transcription	Fetal Kidney	kidney
33	chr10:5903600-5916600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr10:5903800-5905400	Enhancers	Primary B cells from peripheral blood	blood
35	chr10:5903800-5907200	Strong transcription	Fetal Stomach	stomach
36	chr10:5903800-5913600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:5903800-5916000	Weak transcription	NHEK	skin
38	chr10:5903800-5916400	Weak transcription	A549	lung
39	chr10:5903800-5918200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:5904000-5905400	Flanking Active TSS	GM12878-XiMat	blood
41	chr10:5904000-5906000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr10:5904200-5905000	Strong transcription	Brain Angular Gyrus	brain
43	chr10:5904200-5905000	Strong transcription	Ovary	ovary
44	chr10:5904200-5905200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr10:5904200-5906000	Strong transcription	Fetal Intestine Small	intestine
46	chr10:5904400-5905200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:5904400-5916200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:5904400-5916200	Weak transcription	Aorta	Aorta
49	chr10:5904600-5905000	Weak transcription	Thymus	Thymus
50	chr10:5904600-5905200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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