Variant report

Variant	nsv576511
Chromosome Location	chr18:12657247-12658191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr18:12656956-12658031	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr18:12658128-12658361	K562	blood:	n/a	n/a
3	BHLHE40	chr18:12658112-12658339	GM12878	blood:	n/a	n/a
4	BHLHE40	chr18:12658019-12658356	HepG2	liver:	n/a	n/a
5	BHLHE40	chr18:12657711-12657720	HepG2	liver:	n/a	n/a
6	BRCA1	chr18:12657677-12657702	HepG2	liver:	n/a	n/a
7	CBX3	chr18:12656955-12657361	K562	blood:	n/a	n/a
8	CCNT2	chr18:12656952-12658330	K562	blood:	n/a	n/a
9	CEBPB	chr18:12658017-12658217	Hela-S3	cervix:	n/a	n/a
10	CHD1	chr18:12656380-12659102	IMR90	lung:	n/a	n/a
11	CHD2	chr18:12657439-12657480	HepG2	liver:	n/a	n/a
12	CHD2	chr18:12657035-12658381	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr18:12658035-12658519	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr18:12657013-12657382	A549	lung:	n/a	n/a
15	CREB1	chr18:12657351-12657811	K562	blood:	n/a	n/a
16	CREB1	chr18:12656957-12658467	HepG2	liver:	n/a	n/a
17	CREB1	chr18:12657763-12658498	A549	lung:	n/a	n/a
18	CTBP2	chr18:12657860-12658806	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr18:12658160-12658310	SAEC	small airway:	n/a	n/a
20	CTCF	chr18:12658160-12658310	AG09319	gingival:	n/a	n/a
21	CTCF	chr18:12657874-12657948	Fibrobl	skin:	n/a	n/a
22	CTCF	chr18:12658060-12658350	NHEK	skin:	n/a	n/a
23	CTCF	chr18:12658160-12658310	GM12867	blood:	n/a	n/a
24	CTCF	chr18:12658153-12658414	MCF-7	breast:	n/a	n/a
25	CTCF	chr18:12658060-12658210	GM12866	blood:	n/a	n/a
26	CTCF	chr18:12657666-12657711	Fibrobl	skin:	n/a	n/a
27	CTCF	chr18:12657845-12657884	GM13977	blood:	n/a	n/a
28	CTCF	chr18:12657828-12657947	MCF-7	breast:	n/a	n/a
29	CTCF	chr18:12657160-12657310	AG04449	skin:	n/a	n/a
30	CTCF	chr18:12658086-12658345	IMR90	lung:	n/a	n/a
31	CTCF	chr18:12657867-12657875	GM12892	blood:	n/a	n/a
32	CTCF	chr18:12658080-12658230	GM12865	blood:	n/a	n/a
33	CTCF	chr18:12658120-12658270	GM12871	blood:	n/a	n/a
34	CTCF	chr18:12658140-12658290	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr18:12658140-12658348	MCF-7	breast:	n/a	n/a
36	CTCF	chr18:12658148-12658420	GM19238	blood:	n/a	n/a
37	CTCF	chr18:12658180-12658330	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr18:12658140-12658290	AG04449	skin:	n/a	n/a
39	CTCF	chr18:12658160-12658310	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr18:12657160-12657310	SAEC	small airway:	n/a	n/a
41	CTCF	chr18:12658180-12658330	GM12874	blood:	n/a	n/a
42	CTCF	chr18:12658188-12658416	GM12892	blood:	n/a	n/a
43	CTCF	chr18:12658180-12658330	HFF	foreskin:	n/a	n/a
44	CTCF	chr18:12658060-12658210	RPTEC	kidney:	n/a	n/a
45	CTCF	chr18:12658160-12658310	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr18:12657236-12657305	MCF-7	breast:	n/a	n/a
47	CTCF	chr18:12657846-12657961	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:12658160-12658310	BJ	skin:	n/a	n/a
49	CTCF	chr18:12658120-12658270	GM12869	blood:	n/a	n/a
50	CTCF	chr18:12657856-12657910	GM12891	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12657692-12657742	CMK	blood:	n/a
2	chr18:12657909-12657959	GM19239	blood:	n/a
3	chr18:12657692-12657742	HepG2	liver:	n/a
4	chr18:12657909-12657959	CMK	blood:	n/a
5	chr18:12657909-12657959	AG10803	skin:	n/a
6	chr18:12657749-12657799	HCM	heart:	n/a
7	chr18:12657749-12657799	AG04450	lung:	fetal
8	chr18:12657909-12657959	Jurkat	blood:	n/a
9	chr18:12657909-12657959	HCT-116	colon:	n/a
10	chr18:12657909-12657959	GM12891	blood:	n/a
11	chr18:12657909-12657959	HRCEpiC	kidney:	n/a
12	chr18:12657692-12657742	HUVEC	blood vessel:	n/a
13	chr18:12657909-12657959	H1-hESC	embryonic stem cell:	embryo
14	chr18:12657692-12657742	GM12892	blood:	n/a
15	chr18:12657692-12657742	ProgFib	skin:	n/a
16	chr18:12657909-12657959	SK-N-MC	brain:	n/a
17	chr18:12657749-12657799	HEK293	kidney:	embryo
18	chr18:12657692-12657742	HMEC	breast:	n/a
19	chr18:12657749-12657799	AG09309	skin:	n/a
20	chr18:12657692-12657742	HEK293	kidney:	embryo
21	chr18:12657692-12657742	ovcar-3	ovarian:	n/a
22	chr18:12657909-12657959	LNCaP	prostate:	n/a
23	chr18:12657749-12657799	A549	lung:	n/a
24	chr18:12657749-12657799	NT2-D1	testis:	n/a
25	chr18:12657749-12657799	BJ	skin:	n/a
26	chr18:12657692-12657742	AG04449	skin:	fetal
27	chr18:12657692-12657742	GM12878	blood:	n/a
28	chr18:12657909-12657959	HUVEC	blood vessel:	n/a
29	chr18:12657749-12657799	ECC-1	luminal epithelium:	n/a
30	chr18:12657749-12657799	GM12892	blood:	n/a
31	chr18:12657909-12657959	HEEpiC	esophagus:	n/a
32	chr18:12657692-12657742	SK-N-SH	brain:	n/a
33	chr18:12657909-12657959	SK-N-SH	brain:	n/a
34	chr18:12657749-12657799	IMR90	lung:	fetal
35	chr18:12657749-12657799	Caco-2	colon:	n/a
36	chr18:12657749-12657799	Hela-S3	cervix:	n/a
37	chr18:12657692-12657742	ECC-1	luminal epithelium:	n/a
38	chr18:12657692-12657742	Caco-2	colon:	n/a
39	chr18:12657909-12657959	NHBE	bronchial:	n/a
40	chr18:12657909-12657959	AG09319	gingival:	n/a
41	chr18:12657692-12657742	HNPCEpiC	eye:	n/a
42	chr18:12657749-12657799	NHDF-neo	bronchial:	n/a
43	chr18:12657692-12657742	HCT-116	colon:	n/a
44	chr18:12657692-12657742	MCF10A-Er-Src	breast:	n/a
45	chr18:12657749-12657799	U87	brain:	n/a
46	chr18:12657909-12657959	HAEpiC	amniotic membrane:	n/a
47	chr18:12657749-12657799	SKMC	muscle:	n/a
48	chr18:12657909-12657959	HPAEpiC	pulmonary alveolar:	n/a
49	chr18:12657909-12657959	GM12878	blood:	n/a
50	chr18:12657692-12657742	HPAEpiC	pulmonary alveolar:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12657540..12658417-chr22:46475896..46476854,2	Hela-S3	cervix:
2	chr18:12657085..12659648-chr18:12882376..12884207,2	K562	blood:
3	chr18:12406559..12410304-chr18:12656888..12659730,4	MCF-7	breast:
4	chr18:12374049..12378632-chr18:12655494..12660049,8	K562	blood:
5	chr18:12418519..12420831-chr18:12657213..12660140,3	MCF-7	breast:
6	chr18:12372972..12377735-chr18:12656683..12660675,6	K562	blood:
7	chr18:12443233..12445110-chr18:12655911..12658418,2	MCF-7	breast:
8	chr18:12404079..12409500-chr18:12655702..12659746,9	K562	blood:
9	chr18:12648702..12654959-chr18:12655130..12658770,8	K562	blood:
10	chr18:12375564..12378929-chr18:12655169..12659722,7	MCF-7	breast:
11	chr18:12654302..12656873-chr18:12657659..12659911,2	MCF-7	breast:
12	chr18:12375685..12377446-chr18:12655932..12658656,3	MCF-7	breast:
13	chr18:12307735..12310451-chr18:12655693..12658579,2	MCF-7	breast:
14	chr18:12656018..12659900-chr18:12701056..12705601,5	K562	blood:
15	chr18:12657668..12659639-chr18:12701302..12703566,3	MCF-7	breast:
16	chr18:12649857..12654959-chr18:12655130..12658770,11	K562	blood:
17	chr18:12651259..12653780-chr18:12656567..12658681,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000215527	TF binding region
SPIRE1	TF binding region
PSMG2	TF binding region
ENSG00000215527	CpG island
SPIRE1	CpG island
PSMG2	CpG island
ENSG00000101624	chromatin interactions
ENSG00000134278	chromatin interactions
ENSG00000176014	chromatin interactions
ENSG00000197182	chromatin interactions
ENSG00000267199	chromatin interactions
ENSG00000128789	chromatin interactions
ENSG00000175354	chromatin interactions
ENSG00000141391	chromatin interactions
ENSG00000141385	chromatin interactions

Extended variants
information (count: 29 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537753250	chr18:12657251-12657252	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs111822193	chr18:12657291-12657292	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs1105122	chr18:12657320-12657321	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs201043053	chr18:12657334-12657335	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs537631460	chr18:12657353-12657354	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs146027871	chr18:12657384-12657385	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs371514996	chr18:12657429-12657430	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs34472716	chr18:12657431-12657432	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs572065195	chr18:12657457-12657458	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs369751804	chr18:12657481-12657482	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs534365939	chr18:12657483-12657484	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs182090603	chr18:12657633-12657634	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs150658464	chr18:12657642-12657643	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs574335743	chr18:12657643-12657644	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs1058321	chr18:12657712-12657713	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs544916918	chr18:12657742-12657743	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs563215443	chr18:12657788-12657789	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs577954522	chr18:12657855-12657856	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs545094996	chr18:12657888-12657889	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs560600230	chr18:12657999-12658000	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs527793785	chr18:12658006-12658007	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs4073592	chr18:12658045-12658046	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs560748120	chr18:12658055-12658056	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs531444697	chr18:12658067-12658068	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs139943173	chr18:12658075-12658076	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	mRNA abundance
26	rs575232552	chr18:12658108-12658109	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs575078871	chr18:12658123-12658124	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs571238760	chr18:12658189-12658190	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs3902981	chr18:12658191-12658192	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12653800-12670400	Weak transcription	Dnd41	blood
2	chr18:12655400-12657400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr18:12655400-12658200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr18:12655400-12658200	Active TSS	Brain Germinal Matrix	brain
5	chr18:12655400-12658800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr18:12655400-12659000	Active TSS	Brain Angular Gyrus	brain
7	chr18:12655400-12659000	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr18:12655400-12659600	Active TSS	Fetal Brain Female	brain
9	chr18:12655800-12659000	Active TSS	NHLF	lung
10	chr18:12656000-12658600	Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr18:12656000-12658600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr18:12656000-12658600	Active TSS	HepG2	liver
13	chr18:12656000-12658600	Active TSS	NH-A	brain
14	chr18:12656000-12658600	Active TSS	NHEK	skin
15	chr18:12656000-12658800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:12656000-12659000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr18:12656000-12659000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr18:12656000-12659000	Active TSS	HSMM	muscle
19	chr18:12656000-12659200	Active TSS	HSMMtube	muscle
20	chr18:12656200-12658000	Active TSS	K562	blood
21	chr18:12656200-12659400	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr18:12656400-12657400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
23	chr18:12656400-12658600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr18:12656400-12658600	Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr18:12656400-12658600	Active TSS	HMEC	breast
26	chr18:12656400-12658800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr18:12656400-12658800	Active TSS	NHDF-Ad	bronchial
28	chr18:12656400-12659000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr18:12656400-12659000	Active TSS	Stomach Smooth Muscle	stomach
30	chr18:12656400-12659000	Active TSS	A549	lung
31	chr18:12656600-12657400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr18:12656600-12657400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr18:12656600-12657400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
34	chr18:12656600-12657600	Active TSS	Right Atrium	heart
35	chr18:12656600-12658600	Active TSS	Aorta	Aorta
36	chr18:12656600-12658600	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr18:12656600-12658800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr18:12656600-12658800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr18:12656600-12658800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr18:12656600-12658800	Active TSS	Psoas Muscle	Psoas
41	chr18:12656600-12659000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr18:12656600-12659000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr18:12656600-12659000	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr18:12656600-12659000	Active TSS	Muscle Satellite Cultured Cells	--
45	chr18:12656600-12659000	Active TSS	Fetal Muscle Trunk	muscle
46	chr18:12656600-12659000	Active TSS	Fetal Muscle Leg	muscle
47	chr18:12656600-12659000	Active TSS	Right Ventricle	heart
48	chr18:12656600-12659200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr18:12656800-12657400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr18:12656800-12657400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood

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