Variant report

Variant	rs11552171
Chromosome Location	chr12:498529-498530
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PBX3	chr12:498214-499015	A549	lung:	n/a	n/a
2	MAZ	chr12:498165-498985	HepG2	liver:	n/a	n/a
3	REST	chr12:498156-499343	H1-neurons	neurons:	n/a	n/a
4	ELF1	chr12:498202-499000	A549	lung:	n/a	n/a
5	TEAD4	chr12:498350-498979	H1-hESC	embryonic stem cell:	n/a	chr12:498787-498796
6	CREB1	chr12:498299-499026	A549	lung:	n/a	n/a
7	SP1	chr12:498023-499192	A549	lung:	n/a	chr12:498491-498502 chr12:498491-498503 chr12:498491-498503 chr12:498662-498671 chr12:498274-498283 chr12:498492-498506 chr12:498658-498672 chr12:498663-498672 chr12:498493-498502
8	FOXP2	chr12:498407-498917	PFSK-1	brain:	n/a	n/a
9	TAF1	chr12:497917-498680	GM12892	blood:	n/a	n/a
10	CTCF	chr12:498478-498561	MCF-7	breast:	n/a	chr12:498495-498508 chr12:498493-498511
11	STAT3	chr12:498445-498620	MCF10A-Er-Src	breast:	n/a	chr12:498462-498473
12	GABPA	chr12:498008-499143	K562	blood:	n/a	n/a
13	SIN3AK20	chr12:498296-498653	H1-hESC	embryonic stem cell:	n/a	n/a
14	TAF1	chr12:498038-498685	GM12891	blood:	n/a	n/a
15	RCOR1	chr12:498461-498976	K562	blood:	n/a	n/a
16	MYC	chr12:497716-499110	NB4	blood:	n/a	n/a
17	YY1	chr12:497862-498848	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr12:498202-499061	GM10847	blood:	n/a	n/a
19	POLR2A	chr12:498016-499219	H1-neurons	neurons:	n/a	n/a
20	ATF3	chr12:498408-498999	GM12878	blood:	n/a	n/a
21	MYC	chr12:498097-499083	K562	blood:	n/a	n/a
22	USF2	chr12:498423-499055	H1-hESC	embryonic stem cell:	n/a	chr12:498491-498507
23	TBP	chr12:498021-499047	K562	blood:	n/a	n/a
24	POLR2A	chr12:498169-499063	Gliobla	brain:	n/a	n/a
25	ELF1	chr12:498008-499037	GM12878	blood:	n/a	n/a
26	MAX	chr12:498321-499081	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr12:496627-499304	IMR90	lung:	n/a	n/a
28	REST	chr12:498225-498701	PFSK-1	brain:	n/a	n/a
29	SRF	chr12:498227-499208	MCF-7	breast:	n/a	n/a
30	BRCA1	chr12:498301-499078	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr12:497918-499065	GM18951	blood:	n/a	n/a
32	MYC	chr12:498341-498770	K562	blood:	n/a	n/a
33	TEAD4	chr12:498260-499108	ECC-1	luminal epithelium:	n/a	chr12:498787-498796
34	ELF1	chr12:497989-499205	HCT-116	colon:	n/a	n/a
35	HDAC2	chr12:498283-498681	HepG2	liver:	n/a	chr12:498553-498567
36	FOXA1	chr12:498300-499022	HepG2	liver:	n/a	n/a
37	BCL3	chr12:498186-499130	A549	lung:	n/a	chr12:498781-498790 chr12:498492-498501
38	POLR2A	chr12:497660-499115	GM12878	blood:	n/a	n/a
39	GABPA	chr12:497941-499291	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr12:497941-499069	K562	blood:	n/a	n/a
41	FOXA2	chr12:498320-498783	A549	lung:	n/a	n/a
42	POLR2A	chr12:498306-499004	A549	lung:	n/a	n/a
43	NFIC	chr12:498286-499115	HepG2	liver:	n/a	n/a
44	POLR2A	chr12:497739-499255	HepG2	liver:	n/a	n/a
45	TRIM28	chr12:498272-498769	K562	blood:	n/a	n/a
46	YY1	chr12:498131-498663	GM12891	blood:	n/a	n/a
47	POLR2A	chr12:497758-499038	GM12878	blood:	n/a	n/a
48	PML	chr12:498237-499143	K562	blood:	n/a	n/a
49	MAX	chr12:498286-499016	K562	blood:	n/a	n/a
50	MAX	chr12:497995-499095	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:498496-498546	NHDF-neo	bronchial:	n/a
2	chr12:498496-498546	PrEC	prostate:	n/a
3	chr12:498496-498546	NB4	blood:	n/a
4	chr12:498496-498546	K562	blood:	n/a
5	chr12:498496-498546	HepG2	liver:	n/a
6	chr12:498496-498546	NHBE	bronchial:	n/a
7	chr12:498496-498546	HCPEpiC	choroid plexus:	n/a
8	chr12:498496-498546	HL-60	blood:	n/a
9	chr12:498496-498546	NH-A	brain:	n/a
10	chr12:498496-498546	HCF	heart:	n/a
11	chr12:498496-498546	NT2-D1	testis:	n/a
12	chr12:498496-498546	MCF-7	breast:	n/a
13	chr12:498496-498546	HRE	kidney:	n/a
14	chr12:498496-498546	HIPEpiC	eye:	n/a
15	chr12:498496-498546	BJ	skin:	n/a
16	chr12:498496-498546	AG09309	skin:	n/a
17	chr12:498496-498546	HAEpiC	amniotic membrane:	n/a
18	chr12:498496-498546	PFSK-1	brain:	n/a
19	chr12:498496-498546	CMK	blood:	n/a
20	chr12:498496-498546	HUVEC	blood vessel:	n/a
21	chr12:498496-498546	HEK293	kidney:	embryo
22	chr12:498496-498546	ProgFib	skin:	n/a
23	chr12:498496-498546	GM12892	blood:	n/a
24	chr12:498496-498546	GM12891	blood:	n/a
25	chr12:498496-498546	HCM	heart:	n/a
26	chr12:498496-498546	SK-N-SH_RA	brain:	n/a
27	chr12:498496-498546	ovcar-3	ovarian:	n/a
28	chr12:498496-498546	AG09319	gingival:	n/a
29	chr12:498496-498546	MCF10A-Er-Src	breast:	n/a
30	chr12:498496-498546	IMR90	lung:	fetal
31	chr12:498496-498546	AG10803	skin:	n/a
32	chr12:498496-498546	Hela-S3	cervix:	n/a
33	chr12:498496-498546	T-47D	breast:	n/a
34	chr12:498496-498546	SK-N-MC	brain:	n/a
35	chr12:498496-498546	Jurkat	blood:	n/a
36	chr12:498496-498546	U87	brain:	n/a
37	chr12:498496-498546	LNCaP	prostate:	n/a
38	chr12:498496-498546	HRCEpiC	kidney:	n/a
39	chr12:498496-498546	HRPEpiC	eye:	n/a
40	chr12:498496-498546	HCT-116	colon:	n/a
41	chr12:498496-498546	AG04450	lung:	fetal
42	chr12:498496-498546	Caco-2	colon:	n/a
43	chr12:498496-498546	SKMC	muscle:	n/a
44	chr12:498496-498546	H1-hESC	embryonic stem cell:	embryo
45	chr12:498496-498546	GM12878	blood:	n/a
46	chr12:498496-498546	HNPCEpiC	eye:	n/a
47	chr12:498496-498546	SK-N-SH	brain:	n/a
48	chr12:498496-498546	Hepatocyte	liver:	n/a
49	chr12:498496-498546	RPTEC	kidney:	n/a
50	chr12:498496-498546	PANC-1	pancreas:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:498148..498831-chr9:123555275..123555878,2	Hela-S3	cervix:
2	chr1:10002901..10003432-chr12:498459..499050,2	Hela-S3	cervix:
3	chr12:497611..500419-chr12:508788..511712,2	MCF-7	breast:
4	chr12:496401..500895-chr12:509695..513736,6	K562	blood:
5	chr12:498195..499241-chr14:91294171..91295172,4	Hela-S3	cervix:
6	chr12:418157..420807-chr12:497062..498857,2	MCF-7	breast:
7	chr12:498060..499050-chr5:131892887..131893550,2	Hela-S3	cervix:
8	chr12:498062..498901-chr7:5632387..5632898,2	Hela-S3	cervix:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC77-1	chr12:498439-498652	NONHSAT025341

No data

Variant related genes	Relation type
CCDC77	TF binding region
KDM5A	TF binding region
KDM5A	CpG island
CCDC77	CpG island
ENSG00000214654	Chromatin interaction
ENSG00000120647	Chromatin interaction
ENSG00000075618	Chromatin interaction
ENSG00000113522	Chromatin interaction
ENSG00000073614	Chromatin interaction
ENSG00000258884	Chromatin interaction
ENSG00000119402	Chromatin interaction
ENSG00000228150	Chromatin interaction
ENSG00000162441	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1001401	1.00[ASN][1000 genomes]
rs12308942	1.00[ASN][1000 genomes]
rs1550864	1.00[ASN][1000 genomes]
rs16927949	1.00[ASN][1000 genomes]
rs4980820	1.00[ASN][1000 genomes]
rs4980907	1.00[ASN][1000 genomes]
rs6489476	1.00[ASN][1000 genomes]
rs7296772	1.00[ASN][1000 genomes]
rs7313676	1.00[ASN][1000 genomes]
rs74055611	1.00[ASN][1000 genomes]
rs758539	1.00[ASN][1000 genomes]
rs7975247	1.00[ASN][1000 genomes]
rs9739782	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:494800-499600	Active TSS	GM12878-XiMat	blood
2	chr12:495000-499400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr12:495600-499400	Active TSS	K562	blood
4	chr12:495600-499600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr12:495600-499800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:495800-499000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr12:495800-499200	Active TSS	A549	lung
8	chr12:495800-499600	Active TSS	Right Atrium	heart
9	chr12:496000-499000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr12:496000-499000	Active TSS	HMEC	breast
11	chr12:496000-499000	Active TSS	HSMM	muscle
12	chr12:496000-499400	Active TSS	Thymus	Thymus
13	chr12:496000-499400	Active TSS	NHLF	lung
14	chr12:496000-499600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:496200-499000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:496200-499000	Active TSS	Fetal Intestine Large	intestine
17	chr12:496200-499200	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr12:496200-499400	Active TSS	Muscle Satellite Cultured Cells	--
19	chr12:496200-499400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:496200-499400	Active TSS	NHDF-Ad	bronchial
21	chr12:496400-499000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:496400-499000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:496400-499000	Active TSS	Hela-S3	cervix
24	chr12:496400-499000	Active TSS	HSMMtube	muscle
25	chr12:496400-499400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:496400-499400	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr12:496400-499400	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr12:496400-499800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:496600-499000	Active TSS	Primary T cells fromperipheralblood	blood
30	chr12:496600-499000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:496600-499000	Active TSS	Fetal Muscle Leg	muscle
32	chr12:496600-499000	Active TSS	Fetal Stomach	stomach
33	chr12:496600-499200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr12:496600-499200	Active TSS	Right Ventricle	heart
35	chr12:496600-499400	Active TSS	Fetal Intestine Small	intestine
36	chr12:496600-499400	Active TSS	Fetal Thymus	thymus
37	chr12:496600-499600	Active TSS	H1 Cell Line	embryonic stem cell
38	chr12:496800-499000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr12:496800-499000	Active TSS	Colonic Mucosa	Colon
40	chr12:496800-499000	Active TSS	Placenta	Placenta
41	chr12:496800-499000	Active TSS	Left Ventricle	heart
42	chr12:496800-499200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr12:496800-499200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:496800-499200	Active TSS	Aorta	Aorta
45	chr12:496800-499200	Active TSS	Fetal Brain Male	brain
46	chr12:496800-499200	Active TSS	Ovary	ovary
47	chr12:496800-499200	Bivalent/Poised TSS	HepG2	liver
48	chr12:496800-499400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:496800-499400	Active TSS	Fetal Kidney	kidney
50	chr12:496800-499400	Active TSS	Fetal Muscle Trunk	muscle

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