Variant report

Variant	rs72647360
Chromosome Location	chr12:861105-861106
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	EP300	chr12:860096-863739	ECC-1	luminal epithelium:	n/a	chr12:861695-861711 chr12:861144-861158 chr12:861701-861717 chr12:862546-862562 chr12:862543-862559 chr12:861694-861710 chr12:862424-862440 chr12:860262-860276 chr12:861981-861997
2	BCL3	chr12:860231-861162	A549	lung:	n/a	chr12:860448-860461
3	POLR2A	chr12:860244-861288	HepG2	liver:	n/a	n/a
4	SMC3	chr12:861082-864600	Hela-S3	cervix:	n/a	chr12:862368-862378 chr12:862139-862149
5	CHD1	chr12:860407-861266	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr12:861060-861210	HPAF	blood vessel:	n/a	n/a
7	ZNF143	chr12:860319-861862	K562	blood:	n/a	chr12:861352-861362 chr12:861525-861534 chr12:861344-861362 chr12:861523-861532 chr12:861523-861541 chr12:861700-861710 chr12:861631-861646 chr12:861530-861545 chr12:861315-861330 chr12:861348-861358 chr12:861628-861647 chr12:861624-861642
8	KAP1	chr12:859752-861309	HEK293	kidney:	n/a	n/a
9	WRNIP1	chr12:860217-861882	GM12878	blood:	n/a	n/a
10	POLR2A	chr12:861015-861318	H1-hESC	embryonic stem cell:	n/a	n/a
11	MTA3	chr12:860120-861611	GM12878	blood:	n/a	n/a
12	JUN	chr12:861076-861665	K562	blood:	n/a	chr12:861340-861349
13	RFX5	chr12:859693-861973	Hela-S3	cervix:	n/a	chr12:861282-861296 chr12:861284-861293
14	POLR2A	chr12:861095-861297	A549	lung:	n/a	n/a
15	FOSL2	chr12:860055-861306	A549	lung:	n/a	n/a
16	POLR2A	chr12:860171-862105	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr12:860139-863729	Raji	blood:	n/a	n/a
18	MAZ	chr12:859819-864631	IMR90	lung:	n/a	chr12:862215-862225 chr12:861352-861362 chr12:861341-861351 chr12:861704-861714
19	POLR2A	chr12:860026-862179	U87	brain:	n/a	n/a
20	POLR2A	chr12:861080-862587	K562	blood:	n/a	n/a
21	TAF1	chr12:861023-862268	SK-N-SH	brain:	n/a	n/a
22	REST	chr12:860047-863130	H1-neurons	neurons:	n/a	chr12:861971-861984 chr12:862327-862340 chr12:861026-861036 chr12:861935-861948 chr12:861981-861991 chr12:862312-862325 chr12:862215-862228
23	E2F6	chr12:859931-861124	A549	lung:	n/a	chr12:860913-860922
24	TCF7L2	chr12:860252-861846	HCT-116	colon:	n/a	chr12:860829-860839
25	RAD21	chr12:860108-862528	SK-N-SH	brain:	n/a	chr12:862287-862297 chr12:862021-862035 chr12:862285-862297
26	POLR2A	chr12:859451-863515	Hela-S3	cervix:	n/a	n/a
27	MAZ	chr12:861084-862299	HepG2	liver:	n/a	chr12:862215-862225 chr12:861352-861362 chr12:861341-861351 chr12:861704-861714
28	POLR2A	chr12:860120-862250	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr12:860026-862180	U87	brain:	n/a	n/a
30	SMC3	chr12:859893-861948	SK-N-SH	brain:	n/a	chr12:860449-860459 chr12:860791-860798
31	CTCF	chr12:860960-861110	GM12873	blood:	n/a	n/a
32	POLR2A	chr12:861052-862714	MCF10A-Er-Src	breast:	n/a	n/a
33	MAX	chr12:860145-862088	HCT-116	colon:	n/a	chr12:861352-861362 chr12:861341-861351 chr12:861704-861714
34	YY1	chr12:860283-861345	H1-hESC	embryonic stem cell:	n/a	chr12:860468-860482 chr12:860911-860922 chr12:860847-860858
35	POLR2A	chr12:861085-862344	K562	blood:	n/a	n/a
36	POLR2A	chr12:860970-861438	GM12892	blood:	n/a	n/a
37	SMC3	chr12:860155-862058	GM12878	blood:	n/a	chr12:860449-860459 chr12:860791-860798
38	ZNF263	chr12:860234-861538	HEK293-T-REx	kidney:	n/a	chr12:861059-861068
39	POLR2A	chr12:861004-862004	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr12:858746-862577	GM12891	blood:	n/a	n/a
41	CTCF	chr12:861100-861250	HPF	lung:	n/a	n/a
42	ZNF143	chr12:860989-862358	H1-hESC	embryonic stem cell:	n/a	chr12:861352-861362 chr12:861525-861534 chr12:862244-862254 chr12:861344-861362 chr12:861523-861532 chr12:861523-861541 chr12:861700-861710 chr12:861631-861646 chr12:862039-862057 chr12:861530-861545 chr12:861315-861330 chr12:861348-861358 chr12:862224-862242 chr12:861628-861647 chr12:861624-861642
43	POLR2A	chr12:861032-861310	GM12891	blood:	n/a	n/a
44	POLR2A	chr12:859034-862707	GM19099	blood:	n/a	n/a
45	TCF12	chr12:860102-862221	ECC-1	luminal epithelium:	n/a	n/a
46	ELF1	chr12:860165-861885	HCT-116	colon:	n/a	n/a
47	HEY1	chr12:861007-861998	HepG2	liver:	n/a	n/a
48	POLR2A	chr12:860166-863765	GM15510	blood:	n/a	n/a
49	POLR2A	chr12:860938-861328	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr12:861091-862001	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:723353..724122-chr12:860374..861153,4	MCF-7	breast:
2	chr12:562106..562698-chr12:860790..861501,2	MCF-7	breast:
3	chr12:751953..754697-chr12:859970..862221,2	K562	blood:
4	chr12:860830..863519-chr17:56735307..56737869,2	MCF-7	breast:
5	chr12:749128..755954-chr12:858463..864495,7	MCF-7	breast:
6	chr12:858790..861699-chr12:870992..873821,2	K562	blood:
7	chr12:699443..701175-chr12:860085..862730,2	K562	blood:
8	chr12:684050..686927-chr12:859603..861672,3	K562	blood:
9	chr12:739334..741511-chr12:860709..863370,3	MCF-7	breast:
10	chr12:860770..861524-chr9:131102541..131103389,2	Hela-S3	cervix:
11	chr12:860213..861917-chr12:1056995..1059720,2	MCF-7	breast:
12	chr12:751220..755551-chr12:860416..865761,8	K562	blood:
13	chr12:860874..861474-chr8:121823843..121824589,2	HCT-116	colon:
14	chr12:860210..861203-chr12:922611..923577,2	Hela-S3	cervix:
15	chr12:825603..828799-chr12:857363..861650,3	K562	blood:
16	chr12:749727..757562-chr12:858273..868886,17	MCF-7	breast:
17	chr12:858968..861238-chr12:1057237..1058981,2	K562	blood:

Variant related genes	Relation type
WNK1	TF binding region
ENSG00000272502	Chromatin interaction
ENSG00000255825	Chromatin interaction
ENSG00000167114	Chromatin interaction
ENSG00000002016	Chromatin interaction
ENSG00000172164	Chromatin interaction
ENSG00000177406	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000171840	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs12314329	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv898567	chr12:547683-863517	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
13	nsv898568	chr12:547683-969800	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
14	nsv556887	chr12:632240-867504	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers 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	32 gene(s)	inside rSNPs	diseases
15	nsv556890	chr12:662448-1100555	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
16	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
17	nsv1051590	chr12:722215-974773	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
18	nsv541338	chr12:722215-974773	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats 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	26 gene(s)	inside rSNPs	diseases
19	nsv468956	chr12:737230-982321	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking 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	26 gene(s)	inside rSNPs	diseases
20	nsv556893	chr12:737230-982321	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
21	esv2757485	chr12:786238-964551	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv1046707	chr12:792110-910520	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
23	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
24	esv2754685	chr12:835074-936468	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
25	esv2753750	chr12:835074-939480	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
26	esv2753658	chr12:835074-964506	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
27	esv3693103	chr12:837113-971317	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
28	nsv1052402	chr12:848728-874017	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
29	esv1838887	chr12:850288-873533	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
30	nsv556898	chr12:850288-968489	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
31	nsv468959	chr12:850613-922408	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
32	nsv556899	chr12:850613-922408	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
33	nsv1048535	chr12:850878-874017	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
34	nsv518946	chr12:854331-961336	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
35	nsv556900	chr12:854331-968489	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
36	nsv1047237	chr12:855853-874017	Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
37	esv2760688	chr12:855865-876246	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
38	esv3401864	chr12:860716-863564	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 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	chr12:858800-861200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:859200-861400	Flanking Active TSS	Primary T cells from cord blood	blood
3	chr12:859200-865000	Active TSS	Brain Substantia Nigra	brain
4	chr12:859200-866400	Active TSS	K562	blood
5	chr12:859400-865000	Active TSS	GM12878-XiMat	blood
6	chr12:859600-861200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr12:859600-861200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr12:859600-861200	Flanking Active TSS	NHEK	skin
9	chr12:859600-865600	Active TSS	Brain Cingulate Gyrus	brain
10	chr12:859800-861200	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr12:859800-861200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr12:859800-861200	Flanking Active TSS	Osteobl	bone
13	chr12:859800-861400	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr12:859800-861400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr12:859800-861400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:859800-863000	Active TSS	A549	lung
17	chr12:859800-866000	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr12:859800-866200	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr12:859800-866200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr12:860000-861200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr12:860000-861200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:860000-861200	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr12:860000-861400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr12:860000-861400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr12:860000-861400	Flanking Active TSS	HUVEC	blood vessel
26	chr12:860000-863200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:860000-863200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:860000-864600	Active TSS	Aorta	Aorta
29	chr12:860000-864800	Active TSS	Brain Hippocampus Middle	brain
30	chr12:860000-864800	Active TSS	Fetal Kidney	kidney
31	chr12:860000-865000	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr12:860000-865000	Active TSS	Brain Anterior Caudate	brain
33	chr12:860000-865200	Active TSS	H1 Cell Line	embryonic stem cell
34	chr12:860000-865200	Active TSS	H9 Cell Line	embryonic stem cell
35	chr12:860000-867400	Active TSS	Right Atrium	heart
36	chr12:860000-867600	Active TSS	Right Ventricle	heart
37	chr12:860200-863000	Active TSS	Esophagus	oesophagus
38	chr12:860200-863400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:860200-864200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr12:860200-864800	Active TSS	Left Ventricle	heart
41	chr12:860200-864800	Active TSS	Pancreas	Pancrea
42	chr12:860200-865400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:860200-865400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:860200-865400	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr12:860200-865800	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr12:860200-866000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:860200-866400	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:860200-866800	Active TSS	Psoas Muscle	Psoas
49	chr12:860400-861200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr12:860400-861200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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