Variant report

Variant	esv3521615
Chromosome Location	chr11:67507439-67736627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3255)
CpG islands
(count:1466)
Chromatin interactive
region (count:12)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3255 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:67572955-67573090	K562	blood:	n/a	n/a
2	ATF1	chr11:67546855-67547018	K562	blood:	n/a	n/a
3	ATF1	chr11:67525774-67525796	K562	blood:	n/a	n/a
4	ATF3	chr11:67723227-67723408	K562	blood:	n/a	chr11:67723283-67723292
5	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
6	BACH1	chr11:67723212-67723405	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:67548820-67549170	GM12878	blood:	n/a	chr11:67549020-67549031
8	BATF	chr11:67627170-67627405	GM12878	blood:	n/a	n/a
9	BATF	chr11:67644809-67645315	GM12878	blood:	n/a	chr11:67645088-67645096
10	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
11	BATF	chr11:67646855-67647126	GM12878	blood:	n/a	n/a
12	BATF	chr11:67647999-67648547	GM12878	blood:	n/a	n/a
13	BATF	chr11:67648616-67648960	GM12878	blood:	n/a	n/a
14	BATF	chr11:67606914-67607130	GM12878	blood:	n/a	n/a
15	BATF	chr11:67667021-67667379	GM12878	blood:	n/a	n/a
16	BATF	chr11:67648065-67648547	GM12878	blood:	n/a	n/a
17	BATF	chr11:67652428-67652731	GM12878	blood:	n/a	n/a
18	BATF	chr11:67644982-67645399	GM12878	blood:	n/a	chr11:67645088-67645096
19	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
20	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
21	BATF	chr11:67651682-67652098	GM12878	blood:	n/a	n/a
22	BATF	chr11:67675453-67675797	GM12878	blood:	n/a	n/a
23	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
24	BATF	chr11:67706536-67706734	GM12878	blood:	n/a	n/a
25	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
26	BATF	chr11:67548940-67549181	GM12878	blood:	n/a	chr11:67549020-67549031
27	BATF	chr11:67651724-67652105	GM12878	blood:	n/a	n/a
28	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
29	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
30	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
31	BATF	chr11:67646832-67647124	GM12878	blood:	n/a	n/a
32	BATF	chr11:67615409-67615586	GM12878	blood:	n/a	n/a
33	BATF	chr11:67627161-67627468	GM12878	blood:	n/a	n/a
34	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
35	BATF	chr11:67697714-67698270	GM12878	blood:	n/a	n/a
36	BATF	chr11:67675477-67675829	GM12878	blood:	n/a	n/a
37	BATF	chr11:67697656-67698323	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:67697951-67698286	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:67675592-67675748	GM12878	blood:	n/a	chr11:67675704-67675713
41	BCL11A	chr11:67555126-67555504	GM12878	blood:	n/a	chr11:67555323-67555332
42	BCL11A	chr11:67648000-67648549	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:67651645-67652101	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:67555194-67555488	GM12878	blood:	n/a	chr11:67555323-67555332
45	BCL11A	chr11:67710026-67710227	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:67551659-67551843	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:67571942-67572288	GM12878	blood:	n/a	chr11:67572039-67572048
48	BCL11A	chr11:67627160-67627428	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:67557563-67557812	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:67648648-67648946	GM12878	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67573741-67573791	HL-60	blood:	n/a
2	chr11:67734916-67734966	GM12892	blood:	n/a
3	chr11:67573741-67573791	HL-60	blood:	n/a
4	chr11:67734916-67734966	GM12892	blood:	n/a
5	chr11:67723945-67723995	NHBE	bronchial:	n/a
6	chr11:67572716-67572766	HEEpiC	esophagus:	n/a
7	chr11:67722745-67722795	SK-N-SH	brain:	n/a
8	chr11:67734916-67734966	NT2-D1	testis:	n/a
9	chr11:67719813-67719863	AG09319	gingival:	n/a
10	chr11:67726637-67726687	LNCaP	prostate:	n/a
11	chr11:67573103-67573153	AG04450	lung:	fetal
12	chr11:67733632-67733682	NHDF-neo	bronchial:	n/a
13	chr11:67733632-67733682	CMK	blood:	n/a
14	chr11:67653560-67653610	RPTEC	kidney:	n/a
15	chr11:67572716-67572766	Jurkat	blood:	n/a
16	chr11:67733632-67733682	AG09309	skin:	n/a
17	chr11:67656390-67656440	NH-A	brain:	n/a
18	chr11:67734916-67734966	GM12891	blood:	n/a
19	chr11:67722745-67722795	HCF	heart:	n/a
20	chr11:67734916-67734966	A549	lung:	n/a
21	chr11:67734916-67734966	HCM	heart:	n/a
22	chr11:67572729-67572779	HCF	heart:	n/a
23	chr11:67722745-67722795	SAEC	small airway:	n/a
24	chr11:67571294-67571344	MCF-7	breast:	n/a
25	chr11:67559939-67559989	NHDF-neo	bronchial:	n/a
26	chr11:67574013-67574063	ovcar-3	ovarian:	n/a
27	chr11:67656390-67656440	ECC-1	luminal epithelium:	n/a
28	chr11:67572999-67573049	HepG2	liver:	n/a
29	chr11:67572714-67572764	NH-A	brain:	n/a
30	chr11:67722909-67722959	HNPCEpiC	eye:	n/a
31	chr11:67734916-67734966	HRCEpiC	kidney:	n/a
32	chr11:67726637-67726687	PrEC	prostate:	n/a
33	chr11:67571294-67571344	HRCEpiC	kidney:	n/a
34	chr11:67574013-67574063	MCF-7	breast:	n/a
35	chr11:67719813-67719863	HMEC	breast:	n/a
36	chr11:67656357-67656407	SK-N-MC	brain:	n/a
37	chr11:67733632-67733682	HCPEpiC	choroid plexus:	n/a
38	chr11:67574013-67574063	HIPEpiC	eye:	n/a
39	chr11:67571294-67571344	PANC-1	pancreas:	n/a
40	chr11:67721869-67721919	Caco-2	colon:	n/a
41	chr11:67574013-67574063	HNPCEpiC	eye:	n/a
42	chr11:67722909-67722959	HCF	heart:	n/a
43	chr11:67721869-67721919	NHBE	bronchial:	n/a
44	chr11:67723945-67723995	HUVEC	blood vessel:	n/a
45	chr11:67574013-67574063	HRPEpiC	eye:	n/a
46	chr11:67721869-67721919	AG04449	skin:	fetal
47	chr11:67573741-67573791	HRPEpiC	eye:	n/a
48	chr11:67653560-67653610	HRE	kidney:	n/a
49	chr11:67559939-67559989	Caco-2	colon:	n/a
50	chr11:67572988-67573038	NHDF-neo	bronchial:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67571227..67572733-chr3:125634522..125636253,2	MCF-7	breast:
2	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:
3	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:
4	chr1:150551803..150552520-chr11:67572791..67573460,2	Hela-S3	cervix:
5	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
6	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
7	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
8	chr11:67407400..67409857-chr11:67556404..67559360,2	MCF-7	breast:
9	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
10	chr1:8938391..8938936-chr11:67572724..67573509,2	Hela-S3	cervix:
11	chr11:67722873..67723411-chr8:12516978..12517495,2	MCF-7	breast:
12	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFS8-2	chr11:67655624-67655795	ENSG00000251637
2	lnc-NDUFS8-2	chr11:67654222-67654559	l_505_chr11:67645566-67653308_testes
3	lnc-NDUFS8-2	chr11:67673481-67673821	ENSG00000251637
4	lnc-NDUFS8-2	chr11:67645567-67645953	l_505_chr11:67645566-67653308_testes
5	lnc-NDUFV1-7	chr11:67511793-67512116	NONHSAT022465
6	lnc-UNC93B1-3	chr11:67707154-67707245	ENSG00000254610
7	lnc-NDUFS8-2	chr11:67645965-67646246	l_505_chr11:67645566-67653308_testes
8	lnc-NDUFS8-2	chr11:67654061-67654160	ENSG00000251637
9	lnc-NDUFS8-2	chr11:67661350-67661552	XLOC_009181
10	lnc-UNC93B1-8	chr11:67679200-67679534	expReg_chr11_6588_-
11	lnc-NDUFS8-2	chr11:67653917-67654160	XLOC_009181
12	lnc-NDUFV1-2	chr11:67544666-67545111	ENSG00000248509
13	lnc-NDUFS8-6	chr11:67703029-67703397	NONHSAT022485
14	lnc-NDUFV1-2	chr11:67547802-67550430	ENSG00000248509
15	lnc-NDUFS8-2	chr11:67653124-67653308	l_505_chr11:67645566-67653308_testes
16	lnc-NDUFS8-2	chr11:67655621-67655795	XLOC_009181
17	lnc-NDUFS8-2	chr11:67653484-67654125	l_505_chr11:67645566-67653308_testes
18	lnc-NDUFS8-2	chr11:67654932-67654973	XLOC_009181
19	lnc-UNC93B1-3	chr11:67704246-67704462	ENSG00000254610
20	lnc-UNC93B1-3	chr11:67702034-67702179	ENSG00000254610

No data

Variant related genes	Relation type
ENSG00000221553	TF binding region
OR7E11P	TF binding region
ENSG00000251637	TF binding region
ENSG00000255147	TF binding region
ALG1L8P	TF binding region
RNU6-46P	TF binding region
RPS3AP40	TF binding region
FAM86C2P	TF binding region
ENSG00000254792	TF binding region
ENSG00000254610	TF binding region
ENSG00000254883	TF binding region
ENSG00000255230	TF binding region
ENSG00000254850	TF binding region
ENSG00000221553	CpG island
OR7E11P	CpG island
ENSG00000251637	CpG island
ENSG00000255147	CpG island
ALG1L8P	CpG island
RNU6-46P	CpG island
RPS3AP40	CpG island
FAM86C2P	CpG island
ENSG00000254792	CpG island
ENSG00000254610	CpG island
ENSG00000254883	CpG island
ENSG00000255230	CpG island
ENSG00000254850	CpG island
ENSG00000158483	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000171084	chromatin interactions
KIF21B	miRNA target sites
ADAM9	miRNA target sites
TP53	miRNA target sites
TMC7	miRNA target sites
VOPP1	miRNA target sites
ABTB1	miRNA target sites

Extended variants
information (count: 10967 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:10967 , 50 per page) page: 1 2 3 4 5 6 7 ... 220

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532292349	chr11:67507465-67507466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147554706	chr11:67507466-67507467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190776224	chr11:67507477-67507478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529916018	chr11:67507480-67507481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371593685	chr11:67507481-67507482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201906158	chr11:67507497-67507498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559408910	chr11:67507504-67507505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548054897	chr11:67507522-67507523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200136333	chr11:67507523-67507524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182402786	chr11:67507537-67507538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527544871	chr11:67507543-67507544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200769393	chr11:67507555-67507556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377109244	chr11:67507589-67507590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377122563	chr11:67507590-67507591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56169220	chr11:67507591-67507592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552196082	chr11:67507601-67507602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187009828	chr11:67507602-67507603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537985709	chr11:67507608-67507609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190559101	chr11:67507609-67507610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375967725	chr11:67507610-67507611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568430761	chr11:67507618-67507619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10791926	chr11:67507675-67507676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs182784664	chr11:67507677-67507678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10791927	chr11:67507681-67507682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs546515419	chr11:67507692-67507693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530957823	chr11:67507744-67507745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558613924	chr11:67507755-67507756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552488461	chr11:67507759-67507760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4930501	chr11:67507792-67507793	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201987747	chr11:67507801-67507802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4930502	chr11:67507802-67507803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4930503	chr11:67507814-67507815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201402504	chr11:67507845-67507846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187286782	chr11:67507849-67507850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4930504	chr11:67507861-67507862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs4930505	chr11:67507867-67507868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs144993637	chr11:67507883-67507884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35683949	chr11:67507888-67507889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs149906003	chr11:67507891-67507892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113215809	chr11:67507896-67507897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549858450	chr11:67507973-67507974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568547803	chr11:67508028-67508029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535567016	chr11:67508049-67508050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4930506	chr11:67508050-67508051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566254569	chr11:67508051-67508052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540170301	chr11:67508053-67508054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4930507	chr11:67508093-67508094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs149306850	chr11:67508102-67508103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556552796	chr11:67508124-67508125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544199628	chr11:67508125-67508126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	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
Myelofibrosis	22110671	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67499800-67512800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:67499800-67515200	Weak transcription	Right Atrium	heart
3	chr11:67500000-67521400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:67506000-67512600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:67506400-67511600	Weak transcription	Placenta	Placenta
6	chr11:67511000-67513000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:67511200-67512200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:67511200-67513000	Enhancers	Fetal Heart	heart
9	chr11:67511400-67512000	Enhancers	Fetal Muscle Trunk	muscle
10	chr11:67511600-67511800	Enhancers	Left Ventricle	heart
11	chr11:67511600-67512000	Enhancers	Fetal Muscle Leg	muscle
12	chr11:67511600-67512200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:67511600-67512400	Enhancers	Placenta	Placenta
14	chr11:67512000-67512600	Weak transcription	Gastric	stomach
15	chr11:67512400-67512600	Active TSS	Fetal Lung	lung
16	chr11:67512400-67521000	Weak transcription	Placenta	Placenta
17	chr11:67512600-67512800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67512600-67512800	Enhancers	Left Ventricle	heart
19	chr11:67512600-67513000	Flanking Active TSS	Fetal Lung	lung
20	chr11:67512600-67513000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
21	chr11:67512600-67513200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:67512600-67513200	Enhancers	Esophagus	oesophagus
23	chr11:67512600-67513200	ZNF genes & repeats	Fetal Kidney	kidney
24	chr11:67512600-67513200	ZNF genes & repeats	Gastric	stomach
25	chr11:67512600-67513200	Active TSS	Pancreas	Pancrea
26	chr11:67512600-67513200	Enhancers	Spleen	Spleen
27	chr11:67512800-67513000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:67512800-67513200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:67512800-67513200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:67512800-67513200	Bivalent/Poised TSS	NHDF-Ad	bronchial
31	chr11:67513000-67513200	Active TSS	Fetal Lung	lung
32	chr11:67513000-67515600	Weak transcription	Fetal Heart	heart
33	chr11:67513000-67519000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:67513200-67514000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:67513200-67521400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:67513200-67525400	Weak transcription	Fetal Kidney	kidney
37	chr11:67514400-67515400	Enhancers	Primary B cells from peripheral blood	blood
38	chr11:67514600-67515000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:67514800-67515200	Enhancers	Fetal Stomach	stomach
40	chr11:67515200-67515400	Weak transcription	Fetal Stomach	stomach
41	chr11:67515400-67515800	Enhancers	Fetal Stomach	stomach
42	chr11:67515600-67516200	Enhancers	Fetal Heart	heart
43	chr11:67515600-67516600	Enhancers	Colon Smooth Muscle	Colon
44	chr11:67515800-67521200	Weak transcription	Fetal Stomach	stomach
45	chr11:67516200-67521200	Weak transcription	Fetal Heart	heart
46	chr11:67517600-67524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:67521000-67521200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:67521000-67521200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:67521000-67521600	Enhancers	Fetal Muscle Leg	muscle
50	chr11:67521000-67521600	Enhancers	Ovary	ovary

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