Variant report

Variant	nsv976458
Chromosome Location	chr11:64183936-64198230
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:246)
Chromatin interactive
region (count:34)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:64196660-64197020	GM12878	blood:	n/a	n/a
2	CBX3	chr11:64187903-64188228	K562	blood:	n/a	n/a
3	CHD2	chr11:64185815-64185965	K562	blood:	n/a	n/a
4	CTCF	chr11:64188869-64188911	GM10248	blood:	n/a	n/a
5	CTCF	chr11:64192220-64192370	GM12865	blood:	n/a	n/a
6	CTCF	chr11:64187680-64187830	A549	lung:	n/a	n/a
7	E2F4	chr11:64190073-64190127	MCF10A-Er-Src	breast:	n/a	n/a
8	EBF1	chr11:64187595-64187907	GM12878	blood:	n/a	chr11:64187757-64187768 chr11:64187702-64187713
9	EBF1	chr11:64187568-64187825	GM12878	blood:	n/a	chr11:64187757-64187768 chr11:64187702-64187713
10	ELF1	chr11:64183580-64183942	GM12878	blood:	n/a	n/a
11	FOS	chr11:64188757-64189063	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr11:64187713-64187839	MCF10A-Er-Src	breast:	n/a	n/a
13	JUN	chr11:64183930-64184130	HepG2	liver:	n/a	chr11:64184002-64184015 chr11:64184003-64184012
14	JUN	chr11:64187576-64187912	HepG2	liver:	n/a	chr11:64187742-64187755 chr11:64187856-64187864
15	JUND	chr11:64188759-64189026	HepG2	liver:	n/a	chr11:64188896-64188907
16	JUND	chr11:64187567-64187935	HepG2	liver:	n/a	chr11:64187856-64187864
17	JUND	chr11:64183856-64184164	HepG2	liver:	n/a	chr11:64183971-64183982 chr11:64184003-64184012
18	JUND	chr11:64183870-64184028	H1-hESC	embryonic stem cell:	n/a	chr11:64183971-64183982 chr11:64184003-64184012
19	KAP1	chr11:64187461-64188137	U2OS	brain:	n/a	n/a
20	MAX	chr11:64183321-64183950	K562	blood:	n/a	chr11:64183795-64183805
21	MYC	chr11:64188911-64189074	MCF10A-Er-Src	breast:	n/a	n/a
22	NFIC	chr11:64187234-64187844	ECC-1	luminal epithelium:	n/a	n/a
23	NFIC	chr11:64187215-64187890	ECC-1	luminal epithelium:	n/a	n/a
24	NRF1	chr11:64193001-64193002	H1-hESC	embryonic stem cell:	n/a	n/a
25	PAX5	chr11:64183198-64184055	GM12878	blood:	n/a	n/a
26	PBX3	chr11:64196747-64196906	GM12878	blood:	n/a	n/a
27	POLR2A	chr11:64189077-64189087	GM12878	blood:	n/a	n/a
28	POLR2A	chr11:64183305-64183970	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:64183528-64184016	HL-60	blood:	n/a	n/a
30	POLR2A	chr11:64183268-64184070	GM12892	blood:	n/a	n/a
31	RCOR1	chr11:64187355-64187580	K562	blood:	n/a	n/a
32	RCOR1	chr11:64187389-64187589	K562	blood:	n/a	n/a
33	REST	chr11:64183751-64184006	PANC-1	pancreas:	n/a	chr11:64183913-64183922 chr11:64183894-64183903
34	SETDB1	chr11:64187331-64188282	U2OS	brain:	n/a	n/a
35	SETDB1	chr11:64189800-64190270	U2OS	brain:	n/a	n/a
36	STAT3	chr11:64189838-64189893	MCF10A-Er-Src	breast:	n/a	n/a
37	USF2	chr11:64188343-64188389	Hela-S3	cervix:	n/a	chr11:64188344-64188355
38	USF2	chr11:64188888-64189074	Hela-S3	cervix:	n/a	chr11:64188958-64188969
39	YY1	chr11:64188852-64189067	A549	lung:	n/a	n/a
40	YY1	chr11:64188878-64189070	K562	blood:	n/a	n/a
41	ZNF384	chr11:64185410-64185637	K562	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64186601-64186651	GM12891	blood:	n/a
2	chr11:64187747-64187797	HEEpiC	esophagus:	n/a
3	chr11:64186601-64186651	GM12891	blood:	n/a
4	chr11:64187747-64187797	HEEpiC	esophagus:	n/a
5	chr11:64186601-64186651	HIPEpiC	eye:	n/a
6	chr11:64186719-64186769	H1-hESC	embryonic stem cell:	embryo
7	chr11:64186601-64186651	HCPEpiC	choroid plexus:	n/a
8	chr11:64186601-64186651	NB4	blood:	n/a
9	chr11:64187747-64187797	PrEC	prostate:	n/a
10	chr11:64186601-64186651	MCF-7	breast:	n/a
11	chr11:64187747-64187797	SK-N-MC	brain:	n/a
12	chr11:64198213-64198263	HNPCEpiC	eye:	n/a
13	chr11:64198213-64198263	HCM	heart:	n/a
14	chr11:64186601-64186651	HL-60	blood:	n/a
15	chr11:64186719-64186769	HAEpiC	amniotic membrane:	n/a
16	chr11:64187747-64187797	IMR90	lung:	fetal
17	chr11:64198213-64198263	HAEpiC	amniotic membrane:	n/a
18	chr11:64198213-64198263	PANC-1	pancreas:	n/a
19	chr11:64187747-64187797	GM12892	blood:	n/a
20	chr11:64186601-64186651	HAEpiC	amniotic membrane:	n/a
21	chr11:64186601-64186651	SKMC	muscle:	n/a
22	chr11:64186719-64186769	Hepatocyte	liver:	n/a
23	chr11:64186601-64186651	HCT-116	colon:	n/a
24	chr11:64187747-64187797	Caco-2	colon:	n/a
25	chr11:64186719-64186769	CMK	blood:	n/a
26	chr11:64186601-64186651	AG04449	skin:	fetal
27	chr11:64186719-64186769	K562	blood:	n/a
28	chr11:64187747-64187797	SAEC	small airway:	n/a
29	chr11:64186719-64186769	AG10803	skin:	n/a
30	chr11:64198213-64198263	HRCEpiC	kidney:	n/a
31	chr11:64186719-64186769	HCF	heart:	n/a
32	chr11:64186601-64186651	IMR90	lung:	fetal
33	chr11:64187747-64187797	HRE	kidney:	n/a
34	chr11:64186719-64186769	A549	lung:	n/a
35	chr11:64186719-64186769	Hela-S3	cervix:	n/a
36	chr11:64186601-64186651	PANC-1	pancreas:	n/a
37	chr11:64186719-64186769	HNPCEpiC	eye:	n/a
38	chr11:64187747-64187797	GM06990	blood:	n/a
39	chr11:64186601-64186651	RPTEC	kidney:	n/a
40	chr11:64186601-64186651	HRCEpiC	kidney:	n/a
41	chr11:64198213-64198263	SK-N-SH_RA	brain:	n/a
42	chr11:64198213-64198263	Caco-2	colon:	n/a
43	chr11:64198213-64198263	IMR90	lung:	fetal
44	chr11:64187747-64187797	MCF10A-Er-Src	breast:	n/a
45	chr11:64187747-64187797	U87	brain:	n/a
46	chr11:64187747-64187797	CMK	blood:	n/a
47	chr11:64198213-64198263	T-47D	breast:	n/a
48	chr11:64186719-64186769	Jurkat	blood:	n/a
49	chr11:64186601-64186651	HCF	heart:	n/a
50	chr11:64186719-64186769	HCM	heart:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:64184313-64187414..11:64535815-64538326	K562	blood:
2	11:64197420-64206402..11:64415880-64426617	Hela-S3	cervix:
3	11:64184313-64187414..11:64517861-64519906	GM12878	blood:
4	chr11:64189227..64191285-chr11:64196358..64198269,2	K562	blood:
5	11:64184313-64187414..11:64415880-64426617	GM12878	blood:
6	11:64187414-64187725..11:64402707-64415880	Hela-S3	cervix:
7	11:64184313-64187414..11:64523887-64530985	Hela-S3	cervix:
8	11:64187725-64189071..11:64402707-64415880	K562	blood:
9	11:64197420-64206402..11:64523887-64530985	Hela-S3	cervix:
10	11:64184313-64187414..11:64530985-64535815	GM12878	blood:
11	chr11:64189227..64191285-chr11:64196358..64198269,2	K562	blood:
12	11:64184313-64187414..11:64489786-64499245	GM12878	blood:
13	chr11:64198125..64200052-chr11:64263615..64266038,2	K562	blood:
14	11:64184313-64187414..11:64402707-64415880	GM12878	blood:
15	chr11:64196077..64197933-chr11:64215351..64217656,2	MCF-7	breast:
16	11:64184313-64187414..11:64356433-64395036	GM12878	blood:
17	11:64196069-64197420..11:64415880-64426617	Hela-S3	cervix:
18	11:64184313-64187414..11:64519906-64523887	Hela-S3	cervix:
19	11:64184313-64187414..11:64538326-64543055	GM12878	blood:
20	11:64197420-64206402..11:64402707-64415880	H1-hESC	embryonic stem cell:	embryo
21	11:64197420-64206402..11:64501239-64517861	GM12878	blood:
22	chr11:64186214..64187836-chr11:64216111..64217679,2	K562	blood:
23	11:64184313-64187414..11:64426650-64437729	K562	blood:
24	11:64196069-64197420..11:64501239-64517861	Hela-S3	cervix:
25	11:64184313-64187414..11:64642645-64655002	K562	blood:
26	chr11:64197362..64199430-chr11:64200195..64202972,2	MCF-7	breast:
27	11:64197420-64206402..11:64489786-64499245	GM12878	blood:
28	11:64197420-64206402..11:64426650-64437729	K562	blood:
29	chr11:64195038..64195590-chr11:64216879..64217743,2	K562	blood:
30	chr11:64187682..64189589-chr11:64193182..64195315,2	K562	blood:
31	11:64184313-64187414..11:64322633-64349180	Hela-S3	cervix:
32	11:64196069-64197420..11:64402707-64415880	Hela-S3	cervix:
33	11:64184313-64187414..11:64501239-64517861	GM12878	blood:
34	11:64197420-64206402..11:64356433-64395036	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP003774.4.1-1	chr11:64188203-64188544	NONHSAT021995
2	lnc-TRMT112-3	chr11:64187609-64187687	XLOC_009464
3	lnc-AP003774.4.1-1	chr11:64195633-64195670	ENSG00000231492.2
4	lnc-AP003774.4.1-1	chr11:64195633-64195670	XLOC_009158
5	lnc-AP003774.4.1-1	chr11:64188204-64188529	ENSG00000231492.2
6	lnc-AP003774.4.1-1	chr11:64188204-64188528	XLOC_009157
7	lnc-AP003774.4.1-1	chr11:64187863-64188094	XLOC_009157
8	lnc-AP003774.4.1-1	chr11:64188007-64188033	ENSG00000231492.2
9	lnc-AP003774.4.1-1	chr11:64187863-64188094	ENSG00000231492.2
10	lnc-AP003774.4.1-1	chr11:64187862-64188094	NONHSAT021995

No data

Variant related genes	Relation type
ENSG00000231492	TF binding region
ENSG00000231492	CpG island
ENSG00000237410	chromatin interactions
ENSG00000231492	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000168065	chromatin interactions
ENSG00000068831	chromatin interactions
ENSG00000068976	chromatin interactions
ENSG00000197891	chromatin interactions
ENSG00000181908	chromatin interactions
ENSG00000110047	chromatin interactions
ENSG00000230835	chromatin interactions
ENSG00000110076	chromatin interactions
TMEM20	miRNA target sites
TMEM2	miRNA target sites

Extended variants
information (count: 520 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533849655	chr11:64183938-64183939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562790853	chr11:64183939-64183940	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531498573	chr11:64183954-64183955	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs545228806	chr11:64183975-64183976	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150999153	chr11:64183999-64184000	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs497544	chr11:64184104-64184105	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546816344	chr11:64184161-64184162	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560517664	chr11:64184162-64184163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112086187	chr11:64184167-64184168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs56700027	chr11:64184170-64184171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529271804	chr11:64184180-64184181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549232491	chr11:64184267-64184268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569216925	chr11:64184269-64184270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538002550	chr11:64184275-64184276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547557374	chr11:64184308-64184309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570460752	chr11:64184311-64184312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58287963	chr11:64184358-64184359	Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571787720	chr11:64184393-64184394	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs188239539	chr11:64184397-64184398	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs113556992	chr11:64184416-64184417	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs574102782	chr11:64184424-64184425	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs141160144	chr11:64184455-64184456	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs556134418	chr11:64184558-64184559	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs374089739	chr11:64184562-64184563	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs34068194	chr11:64184588-64184589	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs193176974	chr11:64184597-64184598	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs146950926	chr11:64184611-64184612	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs114300239	chr11:64184619-64184620	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs576208625	chr11:64184672-64184673	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs75586540	chr11:64184680-64184681	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs55646341	chr11:64184731-64184732	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs4963222	chr11:64184735-64184736	Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs397935217	chr11:64184743-64184744	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs572174985	chr11:64184778-64184779	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs574727465	chr11:64184783-64184784	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs4963221	chr11:64184786-64184787	Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560399311	chr11:64184787-64184788	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs540318612	chr11:64184802-64184803	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs529211351	chr11:64184833-64184834	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs560258374	chr11:64184855-64184856	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs184565697	chr11:64184897-64184898	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs525826	chr11:64184905-64184906	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs562588986	chr11:64184910-64184911	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs189886887	chr11:64184916-64184917	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs192789204	chr11:64184944-64184945	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs183774063	chr11:64184955-64184956	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs188405142	chr11:64184977-64184978	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs112922207	chr11:64184990-64184991	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs181888940	chr11:64185046-64185047	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs547432794	chr11:64185099-64185100	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Autism	22209245	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64178000-64184200	Weak transcription	Right Atrium	heart
2	chr11:64182400-64184000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr11:64182400-64184000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:64182800-64196000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:64183600-64184000	Enhancers	Gastric	stomach
6	chr11:64183600-64186000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:64183800-64186600	Weak transcription	Placenta	Placenta
8	chr11:64185600-64186200	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:64186000-64186200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:64186600-64187000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:64186600-64188000	Enhancers	Placenta	Placenta
12	chr11:64187400-64187800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr11:64195600-64196600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:64196200-64196400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:64196200-64196600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:64196200-64196800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:64196400-64196600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:64196400-64197200	Enhancers	Fetal Brain Male	brain
19	chr11:64196400-64197600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:64196800-64197000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:64196800-64197000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:64196800-64197800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr11:64197000-64198000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:64197200-64198000	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr11:64197200-64201600	Weak transcription	Fetal Brain Male	brain
26	chr11:64197400-64198600	Bivalent Enhancer	Fetal Lung	lung
27	chr11:64197600-64198200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:64197600-64198200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr11:64197800-64198600	Enhancers	Fetal Heart	heart
30	chr11:64197800-64199000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr11:64198000-64198200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:64198000-64198200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:64198200-64203800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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