Variant report

Variant	rs3803159
Chromosome Location	chr12:510461-510462
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	POLR2A	chr12:510337-511068	GM12891	blood:	n/a	n/a
2	YY1	chr12:510443-511068	K562	blood:	n/a	chr12:510983-510994
3	NFIC	chr12:510432-510982	HepG2	liver:	n/a	n/a
4	POLR2A	chr12:510362-511168	GM19193	blood:	n/a	n/a
5	CEBPD	chr12:510388-511058	HepG2	liver:	n/a	n/a
6	MAX	chr12:510358-511659	A549	lung:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
7	POLR2A	chr12:510369-511026	HepG2	liver:	n/a	n/a
8	POLR2A	chr12:510405-511080	U87	brain:	n/a	n/a
9	POLR2A	chr12:510416-510956	HepG2	liver:	n/a	n/a
10	ELF1	chr12:510390-511025	MCF-7	breast:	n/a	n/a
11	MAX	chr12:510410-510992	K562	blood:	n/a	n/a
12	POLR2A	chr12:510402-511052	GM12878	blood:	n/a	n/a
13	POLR2A	chr12:510351-511080	U87	brain:	n/a	n/a
14	CREB1	chr12:510430-511031	ECC-1	luminal epithelium:	n/a	n/a
15	PML	chr12:510351-511107	K562	blood:	n/a	n/a
16	NFIC	chr12:510408-510997	GM12878	blood:	n/a	n/a
17	SMC3	chr12:510424-511053	Hela-S3	cervix:	n/a	n/a
18	MAX	chr12:510254-511157	HepG2	liver:	n/a	n/a
19	ZBTB33	chr12:510444-510960	GM12878	blood:	n/a	n/a
20	CUX1	chr12:510320-510975	K562	blood:	n/a	n/a
21	CHD2	chr12:510448-511054	HepG2	liver:	n/a	n/a
22	BHLHE40	chr12:510198-511441	K562	blood:	n/a	n/a
23	NRF1	chr12:510431-511134	GM12878	blood:	n/a	n/a
24	MAX	chr12:510379-511578	Hela-S3	cervix:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
25	YY1	chr12:510435-510918	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:510319-511154	PFSK-1	brain:	n/a	n/a
27	MYC	chr12:510356-511595	NB4	blood:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
28	NFYB	chr12:510360-511010	Hela-S3	cervix:	n/a	chr12:510710-510725
29	E2F4	chr12:510424-511122	Hela-S3	cervix:	n/a	chr12:510683-510692
30	CEBPB	chr12:510317-510941	H1-hESC	embryonic stem cell:	n/a	chr12:510496-510509 chr12:510497-510508
31	ELF1	chr12:510359-510985	MCF-7	breast:	n/a	n/a
32	FOXM1	chr12:510230-511231	ECC-1	luminal epithelium:	n/a	n/a
33	TBP	chr12:510444-510996	GM12878	blood:	n/a	n/a
34	FOSL2	chr12:510244-511066	A549	lung:	n/a	chr12:510710-510719
35	POLR2A	chr12:510419-511032	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT5A	chr12:510409-511202	GM12878	blood:	n/a	chr12:510499-510507
37	TBP	chr12:510262-511574	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr12:510431-511197	H1-neurons	neurons:	n/a	n/a
39	BRCA1	chr12:510425-510985	GM12878	blood:	n/a	n/a
40	ATF1	chr12:510436-510930	K562	blood:	n/a	n/a
41	SIN3A	chr12:510371-511713	H1-hESC	embryonic stem cell:	n/a	chr12:511241-511250 chr12:510601-510614
42	POLR2A	chr12:510326-511213	Hela-S3	cervix:	n/a	n/a
43	GTF2F1	chr12:510225-511737	Hela-S3	cervix:	n/a	n/a
44	ETS1	chr12:510352-510949	K562	blood:	n/a	chr12:510626-510639
45	PML	chr12:510243-511170	GM12878	blood:	n/a	n/a
46	SP4	chr12:510374-511047	H1-hESC	embryonic stem cell:	n/a	chr12:510678-510694
47	CEBPB	chr12:510356-510787	HepG2	liver:	n/a	chr12:510496-510509 chr12:510497-510508
48	ZBTB33	chr12:510246-511238	SK-N-SH	brain:	n/a	n/a
49	FOXM1	chr12:510289-511081	GM12878	blood:	n/a	n/a
50	ZBTB33	chr12:510421-510890	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:497611..500419-chr12:508788..511712,2	MCF-7	breast:
2	chr12:508524..511172-chr12:751040..752702,2	MCF-7	breast:
3	chr12:496401..500895-chr12:509695..513736,6	K562	blood:

Variant related genes	Relation type
CCDC77	TF binding region
ENSG00000120647	Chromatin interaction
ENSG00000177406	Chromatin interaction
ENSG00000073614	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1017162	0.81[CHB][hapmap]
rs11062163	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs11062659	0.81[CHB][hapmap]
rs11062769	0.95[AMR][1000 genomes]
rs11834271	0.81[CHB][hapmap]
rs12304242	0.85[CHB][hapmap]
rs12321487	0.93[MEX][hapmap]
rs12321546	0.81[CHB][hapmap];0.83[CHD][hapmap];0.93[MEX][hapmap]
rs16929851	0.81[CHB][hapmap];0.90[CHD][hapmap];1.00[MEX][hapmap]
rs16930401	0.95[AMR][1000 genomes]
rs2053736	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.93[MEX][hapmap]
rs2267988	1.00[EUR][1000 genomes]
rs2284336	0.81[CHB][hapmap];0.90[CHD][hapmap];0.93[MEX][hapmap]
rs2300128	0.81[CHB][hapmap]
rs2887438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3753160	0.81[CHB][hapmap]
rs3803158	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3815557	0.81[CHB][hapmap]
rs4980816	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4980870	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap]
rs4980873	0.84[CHB][hapmap]
rs4980893	0.86[MEX][hapmap];0.80[AMR][1000 genomes]
rs4980894	1.00[EUR][1000 genomes]
rs505631	0.80[CHB][hapmap];0.83[JPT][hapmap]
rs523169	0.83[JPT][hapmap]
rs546796	0.87[JPT][hapmap]
rs548755	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs554597	0.81[JPT][hapmap]
rs57139014	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs720127	0.81[CHB][hapmap]
rs74055616	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051726	chr12:282465-511843	Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv541304	chr12:282465-635505	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1042991	chr12:282465-666255	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1041574	chr12:282465-812000	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	nsv541305	chr12:282465-1016828	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv869390	chr12:282465-1045994	Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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 miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv1050781	chr12:321353-783899	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv1040849	chr12:321619-771493	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	nsv541322	chr12:321619-771493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
12	nsv1035679	chr12:321619-781558	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
13	nsv1053519	chr12:321619-828175	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
15	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
16	esv2757484	chr12:335010-543206	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	esv2759875	chr12:335010-990544	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
18	nsv1045638	chr12:349031-893536	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
19	nsv541325	chr12:349031-893536	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
20	nsv1050646	chr12:362398-658665	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv541326	chr12:362398-658665	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
22	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
23	nsv898565	chr12:428131-564185	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	nsv1052201	chr12:429128-515675	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
25	nsv541328	chr12:429128-515675	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv442250	chr12:432808-543847	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	esv2756520	chr12:433151-543206	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
28	nsv1050226	chr12:441032-743195	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
29	nsv1035222	chr12:449993-515675	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
30	esv2758290	chr12:457433-990544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
31	nsv949226	chr12:493900-814882	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
32	nsv898566	chr12:499041-570917	Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
33	nsv1036822	chr12:504573-586674	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
34	nsv541329	chr12:504573-586674	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
35	nsv514668	chr12:506474-521532	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:509400-511800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:509800-510600	Flanking Active TSS	Dnd41	blood
3	chr12:510000-510600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr12:510000-510600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:510000-510600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:510000-510600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:510000-510600	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr12:510000-510800	Enhancers	Spleen	Spleen
9	chr12:510000-511200	Active TSS	Stomach Smooth Muscle	stomach
10	chr12:510000-511400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:510000-511400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr12:510000-511400	Active TSS	Brain Germinal Matrix	brain
13	chr12:510000-511400	Active TSS	Psoas Muscle	Psoas
14	chr12:510000-511600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:510000-511600	Active TSS	Fetal Intestine Small	intestine
16	chr12:510000-511800	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr12:510000-511800	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr12:510000-511800	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr12:510000-511800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:510000-512000	Active TSS	H1 Cell Line	embryonic stem cell
21	chr12:510000-512000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:510000-512000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:510000-512000	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr12:510000-512000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:510000-512200	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr12:510000-512200	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr12:510000-512200	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr12:510200-510600	Flanking Active TSS	Primary T cells from cord blood	blood
29	chr12:510200-510600	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr12:510200-510600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr12:510200-510600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr12:510200-510600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr12:510200-510600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:510200-510600	Flanking Active TSS	Liver	Liver
35	chr12:510200-510600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr12:510200-510600	Flanking Active TSS	Fetal Muscle Leg	muscle
37	chr12:510200-510600	Flanking Active TSS	Fetal Thymus	thymus
38	chr12:510200-510600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr12:510200-510600	Flanking Active TSS	HMEC	breast
40	chr12:510200-510600	Flanking Active TSS	HUVEC	blood vessel
41	chr12:510200-510600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr12:510200-510600	Flanking Active TSS	NH-A	brain
43	chr12:510200-510600	Flanking Active TSS	NHEK	skin
44	chr12:510200-510600	Flanking Active TSS	Osteobl	bone
45	chr12:510200-511000	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr12:510200-511200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:510200-511200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr12:510200-511200	Active TSS	Brain Cingulate Gyrus	brain
49	chr12:510200-511200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr12:510200-511400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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