Variant report

Variant	rs2701849
Chromosome Location	chr12:65019723-65019724
allele	A/C
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	SMC3	chr12:65019045-65019880	GM12878	blood:	n/a	n/a
2	TBP	chr12:65019136-65019731	HepG2	liver:	n/a	n/a
3	EP300	chr12:65019012-65019896	GM12878	blood:	n/a	chr12:65019242-65019251 chr12:65019642-65019651 chr12:65019244-65019258 chr12:65019238-65019252
4	POLR2A	chr12:65019411-65019777	SK-N-SH	brain:	n/a	n/a
5	RUNX3	chr12:65018942-65019902	GM12878	blood:	n/a	n/a
6	CUX1	chr12:65018844-65019907	K562	blood:	n/a	n/a
7	SP1	chr12:65018851-65020041	A549	lung:	n/a	n/a
8	TAF1	chr12:65019249-65019918	K562	blood:	n/a	n/a
9	USF1	chr12:65018954-65019887	A549	lung:	n/a	chr12:65019469-65019485 chr12:65019646-65019657
10	FOXM1	chr12:65019009-65019752	MCF-7	breast:	n/a	n/a
11	FOS	chr12:65018929-65019837	MCF10A-Er-Src	breast:	n/a	chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019643-65019651 chr12:65019644-65019651 chr12:65019818-65019830 chr12:65019642-65019652
12	MAFK	chr12:65019035-65019854	K562	blood:	n/a	n/a
13	TBL1XR1	chr12:65019240-65019780	K562	blood:	n/a	n/a
14	MYBL2	chr12:65018915-65019794	HepG2	liver:	n/a	n/a
15	CREB1	chr12:65018889-65019947	GM12878	blood:	n/a	n/a
16	MAX	chr12:65018883-65020041	A549	lung:	n/a	chr12:65019642-65019651 chr12:65019643-65019652 chr12:65019647-65019656
17	TBP	chr12:65019065-65019911	GM12878	blood:	n/a	n/a
18	RUNX3	chr12:65018646-65019980	GM12878	blood:	n/a	n/a
19	RELA	chr12:65019084-65019821	GM19193	blood:	n/a	chr12:65019340-65019349 chr12:65019340-65019349
20	CTCF	chr12:65019580-65019730	AG04449	skin:	n/a	n/a
21	GABPA	chr12:65019137-65019837	A549	lung:	n/a	chr12:65019326-65019333
22	MYC	chr12:65018911-65019838	K562	blood:	n/a	chr12:65019642-65019651 chr12:65019643-65019652 chr12:65019647-65019656
23	WRNIP1	chr12:65018947-65019785	GM12878	blood:	n/a	n/a
24	TEAD4	chr12:65018862-65019962	K562	blood:	n/a	n/a
25	BRCA1	chr12:65019057-65019823	Hela-S3	cervix:	n/a	n/a
26	NR2F2	chr12:65018691-65019901	K562	blood:	n/a	n/a
27	REST	chr12:65019289-65019776	PFSK-1	brain:	n/a	chr12:65019479-65019488 chr12:65019456-65019464
28	BHLHE40	chr12:65018993-65019875	K562	blood:	n/a	chr12:65019469-65019485
29	MAX	chr12:65018914-65019960	A549	lung:	n/a	chr12:65019642-65019651 chr12:65019643-65019652 chr12:65019647-65019656
30	CEBPB	chr12:65018845-65019794	A549	lung:	n/a	chr12:65018912-65018920
31	USF1	chr12:65019188-65019848	A549	lung:	n/a	chr12:65019469-65019485 chr12:65019646-65019657
32	FOS	chr12:65019026-65019893	HUVEC	blood vessel:	n/a	chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019643-65019651 chr12:65019644-65019651 chr12:65019818-65019830 chr12:65019642-65019652
33	FOS	chr12:65019001-65019833	MCF10A-Er-Src	breast:	n/a	chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019643-65019651 chr12:65019644-65019651 chr12:65019818-65019830 chr12:65019642-65019652
34	RELA	chr12:65019117-65019823	GM19099	blood:	n/a	chr12:65019340-65019349 chr12:65019340-65019349
35	PML	chr12:65018950-65019795	K562	blood:	n/a	n/a
36	NFIC	chr12:65018857-65019995	GM12878	blood:	n/a	n/a
37	FOSL2	chr12:65018916-65019873	MCF-7	breast:	n/a	chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019387-65019397 chr12:65019643-65019651 chr12:65019644-65019651 chr12:65019818-65019830 chr12:65019642-65019652
38	ELF1	chr12:65019024-65019764	MCF-7	breast:	n/a	chr12:65019242-65019253
39	TAF1	chr12:65019256-65019799	Hela-S3	cervix:	n/a	n/a
40	MYC	chr12:65018967-65019782	MCF10A-Er-Src	breast:	n/a	chr12:65019642-65019651 chr12:65019643-65019652 chr12:65019647-65019656
41	FOXM1	chr12:65019122-65019921	GM12878	blood:	n/a	n/a
42	MXI1	chr12:65019015-65019866	GM12878	blood:	n/a	n/a
43	RFX5	chr12:65018957-65019760	Hela-S3	cervix:	n/a	n/a
44	GATA3	chr12:65018866-65020034	A549	lung:	n/a	chr12:65019256-65019263 chr12:65019255-65019265 chr12:65019252-65019263 chr12:65019256-65019265 chr12:65019256-65019263 chr12:65019256-65019265 chr12:65019256-65019263 chr12:65019249-65019270
45	EGR1	chr12:65019578-65019885	K562	blood:	n/a	n/a
46	IKZF1	chr12:65018778-65019947	GM12878	blood:	n/a	n/a
47	CEBPB	chr12:65018911-65020020	GM12878	blood:	n/a	chr12:65018912-65018920
48	POLR2A	chr12:65019064-65019885	GM12892	blood:	n/a	n/a
49	STAT5A	chr12:65018915-65019954	GM12878	blood:	n/a	chr12:65019642-65019651 chr12:65019343-65019354 chr12:65019643-65019652
50	EBF1	chr12:65018921-65019912	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:65019020..65021619-chr12:65065192..65067422,3	MCF-7	breast:
2	chr12:65019301..65021176-chr12:65062867..65064609,2	K562	blood:
3	chr12:65018082..65020499-chr12:65056309..65058062,2	MCF-7	breast:
4	chr12:65018895..65020884-chr12:65086015..65088325,2	MCF-7	breast:
5	chr12:65010556..65012937-chr12:65017376..65021348,4	K562	blood:
6	chr12:65018029..65021346-chr12:65072247..65076410,6	MCF-7	breast:
7	chr12:65013056..65015741-chr12:65019440..65021647,2	MCF-7	breast:
8	chr12:65018258..65020873-chr12:65068837..65071390,2	MCF-7	breast:
9	chr12:65011462..65014885-chr12:65017332..65020916,6	MCF-7	breast:
10	chr12:65013677..65016643-chr12:65019438..65021046,2	K562	blood:
11	chr12:64844472..64846840-chr12:65019435..65021283,2	MCF-7	breast:
12	chr12:65001678..65008078-chr12:65013108..65023657,17	MCF-7	breast:
13	chr12:65008925..65011325-chr12:65018761..65021697,3	MCF-7	breast:
14	chr12:65019590..65021389-chr12:65024467..65026055,3	K562	blood:
15	chr12:65019263..65021039-chr12:65064985..65067371,4	MCF-7	breast:
16	chr12:65018061..65020835-chr12:65174615..65176151,2	MCF-7	breast:
17	chr12:65001526..65007900-chr12:65015799..65021807,8	K562	blood:

Variant related genes	Relation type
ENSG00000225195	TF binding region
ENSG00000256670	Chromatin interaction
ENSG00000183735	Chromatin interaction
ENSG00000207546	Chromatin interaction
ENSG00000111490	Chromatin interaction
ENSG00000153179	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10784417	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10784418	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11175483	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11175484	1.00[CEU][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1147105	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1147107	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1244869	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1244873	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1244878	0.88[YRI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1245168	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1245169	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1245179	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1245180	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1245181	0.83[CEU][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1245183	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1245184	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1245185	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1245186	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1245187	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1261880	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs1264485	0.92[CHB][hapmap];0.92[JPT][hapmap];0.81[YRI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1268914	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1270437	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1270836	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1270837	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1272547	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1383117	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1690259	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1690272	0.91[CEU][hapmap];0.87[YRI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1690273	0.95[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1716490	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1716496	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1716506	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1716517	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1795613	0.95[ASN][1000 genomes]
rs1795618	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1795621	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1795622	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795624	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795625	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1797677	0.84[JPT][hapmap]
rs1797678	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1797679	0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1797684	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1797688	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1797689	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2464347	0.95[ASN][1000 genomes]
rs2620730	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2682714	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2682716	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2682719	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2682728	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs2701850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7313651	0.88[AFR][1000 genomes]
rs7313765	0.85[JPT][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes]
rs7968403	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7971636	0.95[ASN][1000 genomes]
rs7975455	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832443	chr12:64878856-65057265	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1048199	chr12:64951666-65021700	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
3	nsv541512	chr12:64951666-65021700	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
4	nsv832444	chr12:64981484-65168472	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
5	nsv559203	chr12:65002969-65199922	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv1045216	chr12:65009102-65176894	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv541513	chr12:65009102-65176894	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS 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 miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv469457	chr12:65009243-65195977	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS 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	15 gene(s)	inside rSNPs	diseases
9	nsv559204	chr12:65009243-65195977	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv438218	chr12:65017844-65037483	Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:65006800-65031800	Weak transcription	Dnd41	blood
2	chr12:65010000-65023200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr12:65010800-65022200	Weak transcription	Spleen	Spleen
4	chr12:65016800-65020600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:65017000-65019800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:65017000-65019800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:65017200-65019800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:65017400-65020200	Enhancers	Small Intestine	intestine
9	chr12:65018000-65021200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:65018000-65024600	Weak transcription	Aorta	Aorta
11	chr12:65018200-65019800	Enhancers	Stomach Mucosa	stomach
12	chr12:65018200-65020200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:65018200-65020600	Enhancers	Lung	lung
14	chr12:65018400-65019800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr12:65018400-65020200	Flanking Active TSS	Hela-S3	cervix
16	chr12:65018400-65029200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:65018600-65019800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr12:65018600-65019800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr12:65018600-65019800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:65018600-65019800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr12:65018600-65024800	Weak transcription	Gastric	stomach
22	chr12:65018600-65035000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:65018800-65019800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr12:65018800-65019800	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr12:65018800-65019800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:65018800-65019800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr12:65018800-65019800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr12:65018800-65020000	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr12:65018800-65020000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr12:65018800-65020000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr12:65018800-65020000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:65018800-65020000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr12:65018800-65020000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
34	chr12:65018800-65020000	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr12:65018800-65020000	Flanking Active TSS	HMEC	breast
36	chr12:65018800-65020000	Flanking Active TSS	NHLF	lung
37	chr12:65018800-65020200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr12:65018800-65020200	Flanking Active TSS	HUVEC	blood vessel
39	chr12:65019000-65019800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr12:65019000-65019800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:65019000-65019800	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr12:65019000-65019800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr12:65019000-65019800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr12:65019000-65019800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:65019000-65019800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:65019000-65019800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr12:65019000-65019800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:65019000-65019800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr12:65019000-65019800	Flanking Active TSS	NH-A	brain
50	chr12:65019000-65019800	Flanking Active TSS	NHEK	skin

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