Variant report

Variant	rs144961632
Chromosome Location	chr12:1702971-1702972
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	POLR2A	chr12:1701544-1703295	GM12891	blood:	n/a	n/a
2	ZNF143	chr12:1702949-1703115	Hela-S3	cervix:	n/a	n/a
3	MAZ	chr12:1701409-1704769	IMR90	lung:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
4	TCF3	chr12:1702818-1703558	GM12878	blood:	n/a	n/a
5	GATA3	chr12:1702047-1704421	A549	lung:	n/a	n/a
6	UBTF	chr12:1701676-1704682	K562	blood:	n/a	n/a
7	POLR2A	chr12:1701614-1704251	GM12878	blood:	n/a	n/a
8	ZEB1	chr12:1702467-1703598	HepG2	liver:	n/a	chr12:1703067-1703079 chr12:1702659-1702671
9	POLR2A	chr12:1701802-1704293	MCF-7	breast:	n/a	n/a
10	MAX	chr12:1702649-1704355	NB4	blood:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
11	MAZ	chr12:1702673-1704275	Hela-S3	cervix:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
12	YY1	chr12:1702791-1703692	ECC-1	luminal epithelium:	n/a	chr12:1703253-1703264 chr12:1703269-1703283 chr12:1703263-1703277
13	BCLAF1	chr12:1702596-1703225	GM12878	blood:	n/a	n/a
14	MAX	chr12:1701918-1704587	A549	lung:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
15	SIN3AK20	chr12:1702700-1703568	PANC-1	pancreas:	n/a	n/a
16	E2F6	chr12:1702288-1703474	H1-hESC	embryonic stem cell:	n/a	chr12:1703266-1703275
17	POU2F2	chr12:1702723-1703284	GM12891	blood:	n/a	chr12:1703243-1703255
18	TCF12	chr12:1702905-1703218	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr12:1702960-1703013	Gliobla	brain:	n/a	n/a
20	POLR2A	chr12:1701557-1704680	GM12878	blood:	n/a	n/a
21	MAX	chr12:1702887-1703255	K562	blood:	n/a	chr12:1703239-1703249
22	ZNF263	chr12:1701547-1703312	HEK293-T-REx	kidney:	n/a	chr12:1703261-1703270 chr12:1703236-1703245 chr12:1701882-1701891
23	YY1	chr12:1702764-1704244	GM12892	blood:	n/a	chr12:1703253-1703264 chr12:1703269-1703283 chr12:1703885-1703894 chr12:1704220-1704231 chr12:1703865-1703879 chr12:1703263-1703277
24	MXI1	chr12:1702086-1703169	H1-hESC	embryonic stem cell:	n/a	n/a
25	STAT5A	chr12:1702880-1703348	GM12878	blood:	n/a	n/a
26	POLR2A	chr12:1702698-1703274	GM12891	blood:	n/a	n/a
27	POLR2A	chr12:1702846-1704279	ECC-1	luminal epithelium:	n/a	n/a
28	CHD1	chr12:1701397-1706266	IMR90	lung:	n/a	chr12:1703237-1703247 chr12:1704434-1704444 chr12:1703259-1703269 chr12:1703926-1703936
29	POLR2A	chr12:1701662-1704382	HL-60	blood:	n/a	n/a
30	MAX	chr12:1702860-1704293	Hela-S3	cervix:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
31	POLR2A	chr12:1701747-1704350	GM18526	blood:	n/a	n/a
32	PBX3	chr12:1702518-1703234	A549	lung:	n/a	n/a
33	POLR2A	chr12:1701585-1703296	GM12892	blood:	n/a	n/a
34	ELF1	chr12:1701648-1704313	GM12878	blood:	n/a	chr12:1703240-1703252 chr12:1703814-1703823 chr12:1703285-1703297
35	NFIC	chr12:1702738-1703383	ECC-1	luminal epithelium:	n/a	n/a
36	PAX5	chr12:1702901-1703215	GM12892	blood:	n/a	n/a
37	POLR2A	chr12:1701487-1702973	IMR90	lung:	n/a	n/a
38	CHD2	chr12:1701565-1703513	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269
39	E2F6	chr12:1702721-1703376	A549	lung:	n/a	chr12:1703266-1703275
40	BCL3	chr12:1702811-1703565	GM12878	blood:	n/a	chr12:1703277-1703290 chr12:1703246-1703255 chr12:1703251-1703264
41	POLR2A	chr12:1702709-1703016	GM12878	blood:	n/a	n/a
42	MYC	chr12:1702825-1703266	MCF-7	breast:	n/a	chr12:1703239-1703249
43	CHD2	chr12:1702913-1703012	K562	blood:	n/a	n/a
44	POLR2A	chr12:1702726-1704228	MCF-7	breast:	n/a	n/a
45	MAX	chr12:1702516-1704366	HepG2	liver:	n/a	chr12:1703239-1703249 chr12:1704066-1704075 chr12:1703785-1703795
46	CHD1	chr12:1702663-1704334	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269 chr12:1703926-1703936
47	POLR2A	chr12:1701569-1704320	K562	blood:	n/a	n/a
48	MYC	chr12:1702830-1703333	MCF-7	breast:	n/a	chr12:1703239-1703249
49	CCNT2	chr12:1701679-1704259	K562	blood:	n/a	chr12:1701691-1701700 chr12:1704222-1704231
50	POLR2A	chr12:1701656-1704503	GM19099	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1224466..1226137-chr12:1702484..1704918,2	MCF-7	breast:
2	chr12:547432..549780-chr12:1702241..1704941,2	MCF-7	breast:
3	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:

Variant related genes	Relation type
FBXL14	TF binding region
ENSG00000082805	Chromatin interaction
ENSG00000002016	Chromatin interaction
ENSG00000120647	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:46 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1042863	chr12:1163817-1902302	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv541345	chr12:1163817-1902302	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	esv3397478	chr12:1535455-1730159	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv898584	chr12:1607390-1783251	Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv826180	chr12:1614395-1759431	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv826181	chr12:1619798-1754941	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv898586	chr12:1690140-1734365	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv556979	chr12:1700134-1704325	Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
10	esv3438770	chr12:1701716-1704664	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
11	nsv556980	chr12:1702470-1703520	Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
12	esv1798253	chr12:1702470-1703733	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
13	esv1808280	chr12:1702470-1703733	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
14	esv1819552	chr12:1702470-1703733	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
15	esv1824213	chr12:1702470-1703733	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
16	esv1839926	chr12:1702470-1703733	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
17	esv1840137	chr12:1702470-1703733	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
18	esv1841419	chr12:1702470-1703733	Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
19	esv1841651	chr12:1702470-1703733	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
20	esv1845404	chr12:1702470-1703733	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
21	esv1851029	chr12:1702470-1703733	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
22	nsv556981	chr12:1702470-1703733	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
23	esv1841836	chr12:1702470-1703953	Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
24	nsv556982	chr12:1702470-1703953	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
25	esv1841842	chr12:1702470-1704096	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
26	nsv556983	chr12:1702470-1704096	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
27	nsv556984	chr12:1702470-1704205	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
28	esv1793457	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
29	esv1793746	chr12:1702470-1704325	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
30	esv1799354	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
31	esv1820484	chr12:1702470-1704325	Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
32	esv1834585	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
33	esv1836763	chr12:1702470-1704325	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
34	esv1837561	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
35	esv1839669	chr12:1702470-1704325	Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
36	esv1844404	chr12:1702470-1704325	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
37	nsv556985	chr12:1702470-1704325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
38	nsv556986	chr12:1702470-1705852	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
39	esv18273	chr12:1702491-1704405	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
40	esv3403028	chr12:1702616-1704989	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
41	nsv556987	chr12:1702707-1703733	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
42	nsv556988	chr12:1702707-1703953	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
43	nsv556989	chr12:1702707-1704096	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
44	nsv556990	chr12:1702707-1704205	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
45	nsv556991	chr12:1702913-1703953	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
46	nsv556992	chr12:1702913-1704205	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 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	chr12:1699200-1703200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:1699400-1703000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
3	chr12:1699400-1703000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
4	chr12:1699400-1703000	Flanking Active TSS	Osteobl	bone
5	chr12:1699600-1703200	Flanking Active TSS	HMEC	breast
6	chr12:1699800-1703000	Transcr. at gene 5' and 3'	Dnd41	blood
7	chr12:1699800-1703200	Flanking Active TSS	HUVEC	blood vessel
8	chr12:1700000-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:1700400-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:1700400-1703200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr12:1700600-1703000	Flanking Active TSS	K562	blood
12	chr12:1700600-1703200	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr12:1700600-1704400	Active TSS	Brain Germinal Matrix	brain
14	chr12:1700800-1703000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr12:1700800-1703000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
16	chr12:1700800-1703000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr12:1700800-1703000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
18	chr12:1700800-1704600	Active TSS	Ovary	ovary
19	chr12:1701000-1703000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:1701000-1704800	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr12:1701200-1703200	Active TSS	Stomach Mucosa	stomach
22	chr12:1701200-1704200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr12:1701400-1703000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr12:1701400-1703000	Flanking Active TSS	NHEK	skin
25	chr12:1701400-1703200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:1701400-1703200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:1701600-1703000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:1701600-1703000	Flanking Active TSS	Primary B cells from peripheral blood	blood
32	chr12:1701600-1703000	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr12:1701600-1703000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
34	chr12:1701600-1703000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:1701600-1703000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:1701600-1703000	Flanking Active TSS	Liver	Liver
37	chr12:1701600-1703000	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr12:1701600-1703000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr12:1701600-1703000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr12:1701600-1703000	Flanking Active TSS	Right Ventricle	heart
41	chr12:1701600-1703000	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr12:1701600-1703200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr12:1701600-1703200	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr12:1701600-1703200	Flanking Active TSS	Colonic Mucosa	Colon
45	chr12:1701600-1703200	Flanking Active TSS	Placenta	Placenta
46	chr12:1701600-1703200	Flanking Active TSS	NH-A	brain
47	chr12:1701800-1703000	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr12:1701800-1703000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr12:1701800-1703000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:1701800-1703000	Flanking Active TSS	Spleen	Spleen

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