Variant report

Variant	rs10165968
Chromosome Location	chr2:39350851-39350852
allele	A/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	MTA3	chr2:39350712-39351265	GM12878	blood:	n/a	n/a
2	E2F6	chr2:39350683-39351870	K562	blood:	n/a	chr2:39351466-39351475 chr2:39351640-39351649 chr2:39351702-39351709 chr2:39351489-39351500
3	RELA	chr2:39350831-39351972	GM15510	blood:	n/a	n/a
4	MAX	chr2:39350734-39351994	A549	lung:	n/a	chr2:39351384-39351394 chr2:39351634-39351644
5	POLR2A	chr2:39350829-39352215	ProgFib	skin:	n/a	n/a
6	POLR2A	chr2:39350640-39351963	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr2:39350681-39352203	GM12892	blood:	n/a	n/a
8	UBTF	chr2:39350799-39352177	K562	blood:	n/a	n/a
9	CHD1	chr2:39350835-39351982	H1-hESC	embryonic stem cell:	n/a	chr2:39351702-39351709
10	MXI1	chr2:39350678-39352518	SK-N-SH	brain:	n/a	n/a
11	POLR2A	chr2:39350799-39351988	HepG2	liver:	n/a	n/a
12	POLR2A	chr2:39350803-39352213	HepG2	liver:	n/a	n/a
13	ZKSCAN1	chr2:39350783-39351935	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr2:39350677-39352206	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr2:39350796-39351912	GM18526	blood:	n/a	n/a
16	POLR2A	chr2:39350782-39352093	U87	brain:	n/a	n/a
17	POLR2A	chr2:39350527-39352608	SK-N-MC	brain:	n/a	n/a
18	POLR2A	chr2:39350610-39351949	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr2:39350783-39352426	GM12878	blood:	n/a	n/a
20	RUNX3	chr2:39350809-39352095	GM12878	blood:	n/a	n/a
21	POLR2A	chr2:39350821-39352171	K562	blood:	n/a	n/a
22	ATF3	chr2:39350803-39351660	A549	lung:	n/a	chr2:39351640-39351649
23	CREB1	chr2:39350754-39352204	HepG2	liver:	n/a	n/a
24	HCFC1	chr2:39350753-39352161	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr2:39350804-39352311	K562	blood:	n/a	n/a
26	TEAD4	chr2:39350718-39352250	HepG2	liver:	n/a	n/a
27	PML	chr2:39350832-39352272	K562	blood:	n/a	n/a
28	POLR2A	chr2:39350615-39352362	Raji	blood:	n/a	n/a
29	TCF12	chr2:39350668-39352155	A549	lung:	n/a	n/a
30	CBX3	chr2:39350587-39352120	K562	blood:	n/a	n/a
31	POLR2A	chr2:39350778-39352067	PFSK-1	brain:	n/a	n/a
32	POLR2A	chr2:39350672-39352076	HepG2	liver:	n/a	n/a
33	WRNIP1	chr2:39350804-39352209	GM12878	blood:	n/a	n/a
34	POLR2A	chr2:39350811-39351873	HUVEC	blood vessel:	n/a	n/a
35	PML	chr2:39350742-39351994	K562	blood:	n/a	n/a
36	NR2F2	chr2:39350786-39351990	K562	blood:	n/a	n/a
37	POLR2A	chr2:39350801-39352176	GM19099	blood:	n/a	n/a
38	POLR2A	chr2:39350832-39351919	GM12878	blood:	n/a	n/a
39	SP1	chr2:39350812-39351971	A549	lung:	n/a	chr2:39351641-39351650 chr2:39351639-39351651 chr2:39351640-39351649 chr2:39351639-39351651 chr2:39351640-39351650
40	TAF1	chr2:39350730-39352257	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr2:39350830-39352453	PBDE	blood:	n/a	n/a
42	MYC	chr2:39350797-39352216	K562	blood:	n/a	chr2:39351384-39351394 chr2:39351634-39351644
43	MBD4	chr2:39350672-39352130	HepG2	liver:	n/a	n/a
44	POLR2A	chr2:39350827-39352172	GM18505	blood:	n/a	n/a
45	POLR2A	chr2:39350767-39351985	GM12892	blood:	n/a	n/a
46	POLR2A	chr2:39350721-39352004	HL-60	blood:	n/a	n/a
47	NR2F2	chr2:39350772-39352088	K562	blood:	n/a	n/a
48	GATA3	chr2:39350756-39352033	A549	lung:	n/a	n/a
49	JUND	chr2:39350811-39352039	K562	blood:	n/a	n/a
50	POLR2A	chr2:39350782-39352087	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:38975187..38978600-chr2:39347007..39351369,4	K562	blood:
2	chr2:39350652..39354915-chr2:39355009..39358498,5	K562	blood:
3	chr2:39349857..39351407-chr2:39664055..39665956,2	MCF-7	breast:
4	chr2:39350652..39353712-chr2:39355009..39357216,3	K562	blood:
5	chr2:39348643..39351321-chr3:122101958..122103520,2	MCF-7	breast:
6	chr2:39348043..39352382-chr2:39450241..39456710,6	K562	blood:
7	chr10:31320984..31323881-chr2:39349698..39351408,2	MCF-7	breast:

Variant related genes	Relation type
SOS1	TF binding region
ENSG00000202309	Chromatin interaction
ENSG00000114023	Chromatin interaction
ENSG00000160124	Chromatin interaction
ENSG00000115875	Chromatin interaction
ENSG00000011566	Chromatin interaction
ENSG00000205111	Chromatin interaction
ENSG00000231312	Chromatin interaction

Extended variants
information (count: 136 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10153761	0.84[EUR][1000 genomes]
rs10166395	1.00[CEU][hapmap]
rs10166801	0.82[EUR][1000 genomes]
rs10169337	0.80[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap]
rs10172085	0.82[EUR][1000 genomes]
rs10172714	0.83[GIH][hapmap]
rs10177250	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10184015	0.87[EUR][1000 genomes]
rs10190377	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs10194374	0.82[EUR][1000 genomes]
rs10200058	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10201980	0.86[GIH][hapmap]
rs10205802	0.80[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap]
rs10206751	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs1037495	1.00[CEU][hapmap];0.93[CHB][hapmap];0.82[JPT][hapmap]
rs1043793	1.00[CEU][hapmap];0.90[GIH][hapmap]
rs10439459	0.84[EUR][1000 genomes]
rs11124659	0.84[EUR][1000 genomes]
rs11124660	0.89[EUR][1000 genomes]
rs11692687	0.84[EUR][1000 genomes]
rs12471731	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[TSI][hapmap]
rs12620003	1.00[CEU][hapmap];0.89[CHB][hapmap];0.88[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12620071	0.87[EUR][1000 genomes]
rs12622969	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13031871	0.88[CEU][hapmap];0.87[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs13033392	0.92[EUR][1000 genomes]
rs1377860	0.82[GIH][hapmap];0.87[EUR][1000 genomes]
rs1377861	0.87[EUR][1000 genomes]
rs1377863	0.84[EUR][1000 genomes]
rs1377864	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs1454223	0.83[GIH][hapmap]
rs1454226	0.84[EUR][1000 genomes]
rs1454227	0.90[EUR][1000 genomes]
rs1470914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes]
rs1470915	0.90[GIH][hapmap];0.84[EUR][1000 genomes]
rs1869513	0.83[GIH][hapmap]
rs2060987	0.83[GIH][hapmap];0.82[TSI][hapmap]
rs2060988	0.80[ASW][hapmap];0.80[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.82[YRI][hapmap];0.82[EUR][1000 genomes]
rs2060989	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs212322	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2123876	0.80[EUR][1000 genomes]
rs2123879	0.80[EUR][1000 genomes]
rs2123881	0.84[EUR][1000 genomes]
rs2123882	0.89[EUR][1000 genomes]
rs2168042	0.86[CHB][hapmap]
rs2168043	0.93[CHB][hapmap];0.90[CHD][hapmap];0.85[GIH][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs2305516	0.90[GIH][hapmap]
rs2373474	0.82[EUR][1000 genomes]
rs2373495	0.80[EUR][1000 genomes]
rs2373496	0.80[EUR][1000 genomes]
rs2373497	1.00[CHB][hapmap];0.86[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs2888585	0.86[CHB][hapmap];0.84[EUR][1000 genomes]
rs2924714	0.87[EUR][1000 genomes]
rs2969763	0.87[EUR][1000 genomes]
rs297120	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.89[TSI][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs297121	0.87[EUR][1000 genomes]
rs297124	0.81[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs297125	0.87[EUR][1000 genomes]
rs297127	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs297128	0.87[EUR][1000 genomes]
rs297129	0.87[EUR][1000 genomes]
rs297130	0.87[EUR][1000 genomes]
rs297131	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs297132	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs297133	0.87[EUR][1000 genomes]
rs297134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs297135	0.86[CHB][hapmap];0.87[EUR][1000 genomes]
rs297136	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs297137	0.87[EUR][1000 genomes]
rs297139	0.87[EUR][1000 genomes]
rs297140	0.87[EUR][1000 genomes]
rs297141	0.87[EUR][1000 genomes]
rs297142	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs297143	0.87[EUR][1000 genomes]
rs297144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs297145	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs297147	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs297148	0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs297149	0.85[CHB][hapmap];0.87[EUR][1000 genomes]
rs297150	0.86[CHB][hapmap];0.96[GIH][hapmap];0.87[EUR][1000 genomes]
rs297151	0.88[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs297152	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs297153	0.86[CHB][hapmap];0.87[EUR][1000 genomes]
rs297155	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs297156	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs297157	0.87[EUR][1000 genomes]
rs297158	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs297159	0.87[EUR][1000 genomes]
rs297160	0.85[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs297161	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs297162	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs366840	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3765058	0.93[GIH][hapmap]
rs378698	0.86[CHB][hapmap];0.87[EUR][1000 genomes]
rs3796038	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes]
rs388958	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4670269	0.88[CEU][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap]
rs4670272	0.80[EUR][1000 genomes]
rs4670902	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap]
rs4670905	0.87[EUR][1000 genomes]
rs57378308	0.89[EUR][1000 genomes]
rs58645871	0.80[EUR][1000 genomes]
rs59732351	0.89[EUR][1000 genomes]
rs61405040	0.87[EUR][1000 genomes]
rs6419600	1.00[CEU][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6544183	0.90[GIH][hapmap]
rs6544185	0.93[GIH][hapmap]
rs6544191	0.87[EUR][1000 genomes]
rs6544197	0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs6713281	0.90[GIH][hapmap];0.84[EUR][1000 genomes]
rs6725356	0.83[GIH][hapmap];0.82[EUR][1000 genomes]
rs6725644	0.82[EUR][1000 genomes]
rs6726833	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6739807	0.81[EUR][1000 genomes]
rs6756184	0.80[EUR][1000 genomes]
rs6758330	0.82[ASW][hapmap];0.80[CEU][hapmap];0.93[CHB][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.81[LWK][hapmap];0.82[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.84[EUR][1000 genomes]
rs72909662	0.89[EUR][1000 genomes]
rs7571052	0.93[GIH][hapmap]
rs7577088	0.93[GIH][hapmap]
rs7607509	0.80[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap]
rs963730	1.00[CEU][hapmap]
rs970409	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755359	chr2:39169049-39417849	Strong transcription Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv873885	chr2:39200198-39573521	Enhancers Strong transcription Weak transcription Flanking Active TSS 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	36 gene(s)	inside rSNPs	diseases
3	nsv1010874	chr2:39255376-39604535	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv535649	chr2:39255376-39604535	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	nsv531346	chr2:39263225-39606367	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
6	nsv533348	chr2:39264345-39596169	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv1014520	chr2:39270598-39596299	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
8	nsv535650	chr2:39270598-39596299	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
9	nsv1008198	chr2:39271472-39364035	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv1009379	chr2:39271472-39604535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	nsv581493	chr2:39277851-39547575	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv581494	chr2:39277851-39626388	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
13	nsv533456	chr2:39281834-39596298	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
14	nsv581495	chr2:39282079-39475205	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs10165968	TMEM178	cis	cerebellum	SCAN
rs10165968	SOS1	Cis_1M	lymphoblastoid	RTeQTL
rs10165968	SOS1	cis	multi-tissue	Pritchard
rs10165968	SOS1	cis	lymphoblastoid	seeQTL
rs10165968	C2orf58	cis	parietal	SCAN
rs10165968	DHX57	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39348600-39351000	Weak transcription	Gastric	stomach
2	chr2:39348800-39351000	Weak transcription	Ovary	ovary
3	chr2:39349000-39351000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:39349000-39351000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr2:39349000-39351000	Weak transcription	Right Ventricle	heart
6	chr2:39349000-39351000	Enhancers	Stomach Mucosa	stomach
7	chr2:39349200-39351000	Flanking Active TSS	HepG2	liver
8	chr2:39350000-39351000	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr2:39350000-39351200	Flanking Active TSS	Dnd41	blood
10	chr2:39350000-39352200	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr2:39350000-39352600	Active TSS	H9 Cell Line	embryonic stem cell
12	chr2:39350200-39351000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:39350200-39352200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:39350200-39352600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr2:39350400-39351000	Enhancers	Placenta Amnion	Placenta Amnion
16	chr2:39350400-39352200	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr2:39350400-39352200	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr2:39350400-39352400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:39350400-39352600	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr2:39350400-39353000	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr2:39350600-39351000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:39350600-39351000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr2:39350600-39351000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:39350600-39351000	Enhancers	Spleen	Spleen
25	chr2:39350600-39351200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:39350600-39351200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:39350600-39351200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:39350600-39351200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr2:39350600-39351200	Flanking Active TSS	A549	lung
30	chr2:39350600-39351200	Flanking Active TSS	Hela-S3	cervix
31	chr2:39350600-39351400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:39350600-39351400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr2:39350600-39351400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:39350600-39351400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:39350600-39351400	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr2:39350600-39351400	Flanking Active TSS	Liver	Liver
37	chr2:39350600-39351400	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr2:39350600-39351400	Flanking Active TSS	Fetal Muscle Trunk	muscle
39	chr2:39350600-39351400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr2:39350600-39351400	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr2:39350600-39351400	Flanking Active TSS	HMEC	breast
42	chr2:39350600-39352000	Active TSS	HSMM	muscle
43	chr2:39350600-39352200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:39350600-39352400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr2:39350600-39352400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr2:39350600-39352800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:39350600-39352800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:39350800-39351000	Active TSS	H1 Cell Line	embryonic stem cell
49	chr2:39350800-39351000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:39350800-39351000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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