Variant report

Variant	nsv1045024
Chromosome Location	chr11:67550395-67749246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3184)
CpG islands
(count:1588)
Chromatin interactive
region (count:12)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3184 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

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	ATF3	chr11:67723227-67723408	K562	blood:	n/a	chr11:67723283-67723292
3	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
4	BACH1	chr11:67746647-67746690	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:67723212-67723405	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:67652428-67652731	GM12878	blood:	n/a	n/a
7	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
8	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
9	BATF	chr11:67627170-67627405	GM12878	blood:	n/a	n/a
10	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
11	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
12	BATF	chr11:67667021-67667379	GM12878	blood:	n/a	n/a
13	BATF	chr11:67648065-67648547	GM12878	blood:	n/a	n/a
14	BATF	chr11:67648616-67648960	GM12878	blood:	n/a	n/a
15	BATF	chr11:67746466-67746780	GM12878	blood:	n/a	n/a
16	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
17	BATF	chr11:67697714-67698270	GM12878	blood:	n/a	n/a
18	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
19	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
20	BATF	chr11:67615409-67615586	GM12878	blood:	n/a	n/a
21	BATF	chr11:67675477-67675829	GM12878	blood:	n/a	n/a
22	BATF	chr11:67647999-67648547	GM12878	blood:	n/a	n/a
23	BATF	chr11:67651682-67652098	GM12878	blood:	n/a	n/a
24	BATF	chr11:67646855-67647126	GM12878	blood:	n/a	n/a
25	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
26	BATF	chr11:67606914-67607130	GM12878	blood:	n/a	n/a
27	BATF	chr11:67644809-67645315	GM12878	blood:	n/a	chr11:67645088-67645096
28	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
29	BATF	chr11:67627161-67627468	GM12878	blood:	n/a	n/a
30	BATF	chr11:67706536-67706734	GM12878	blood:	n/a	n/a
31	BATF	chr11:67675453-67675797	GM12878	blood:	n/a	n/a
32	BATF	chr11:67697656-67698323	GM12878	blood:	n/a	n/a
33	BATF	chr11:67644982-67645399	GM12878	blood:	n/a	chr11:67645088-67645096
34	BATF	chr11:67651724-67652105	GM12878	blood:	n/a	n/a
35	BATF	chr11:67646832-67647124	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:67571942-67572288	GM12878	blood:	n/a	chr11:67572039-67572048
37	BCL11A	chr11:67697965-67698299	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:67572576-67572779	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:67556040-67556201	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:67675558-67675816	GM12878	blood:	n/a	chr11:67675704-67675713
42	BCL11A	chr11:67648648-67648946	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:67627160-67627428	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:67555194-67555488	GM12878	blood:	n/a	chr11:67555323-67555332
45	BCL11A	chr11:67559730-67560046	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:67555126-67555504	GM12878	blood:	n/a	chr11:67555323-67555332
47	BCL11A	chr11:67571899-67572434	GM12878	blood:	n/a	chr11:67572039-67572048
48	BCL11A	chr11:67601358-67601522	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:67645219-67645410	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:67651645-67652101	GM12878	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67572999-67573049	CMK	blood:	n/a
2	chr11:67656357-67656407	AG04450	lung:	fetal
3	chr11:67572999-67573049	CMK	blood:	n/a
4	chr11:67656357-67656407	AG04450	lung:	fetal
5	chr11:67559939-67559989	SK-N-SH	brain:	n/a
6	chr11:67733632-67733682	AG04450	lung:	fetal
7	chr11:67722909-67722959	ProgFib	skin:	n/a
8	chr11:67745999-67746049	ProgFib	skin:	n/a
9	chr11:67572988-67573038	HNPCEpiC	eye:	n/a
10	chr11:67559939-67559989	GM12878	blood:	n/a
11	chr11:67656357-67656407	SK-N-SH_RA	brain:	n/a
12	chr11:67722745-67722795	Hepatocyte	liver:	n/a
13	chr11:67745999-67746049	NHBE	bronchial:	n/a
14	chr11:67568593-67568643	SK-N-MC	brain:	n/a
15	chr11:67572999-67573049	ovcar-3	ovarian:	n/a
16	chr11:67722745-67722795	NB4	blood:	n/a
17	chr11:67733632-67733682	HL-60	blood:	n/a
18	chr11:67568593-67568643	AG04449	skin:	fetal
19	chr11:67733632-67733682	HRCEpiC	kidney:	n/a
20	chr11:67573103-67573153	HEK293	kidney:	embryo
21	chr11:67574013-67574063	SK-N-MC	brain:	n/a
22	chr11:67721869-67721919	IMR90	lung:	fetal
23	chr11:67723411-67723461	HUVEC	blood vessel:	n/a
24	chr11:67745999-67746049	Jurkat	blood:	n/a
25	chr11:67573741-67573791	BJ	skin:	n/a
26	chr11:67573741-67573791	A549	lung:	n/a
27	chr11:67573103-67573153	SAEC	small airway:	n/a
28	chr11:67653560-67653610	NH-A	brain:	n/a
29	chr11:67572729-67572779	HNPCEpiC	eye:	n/a
30	chr11:67559939-67559989	ProgFib	skin:	n/a
31	chr11:67745999-67746049	SAEC	small airway:	n/a
32	chr11:67571294-67571344	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:67726637-67726687	PANC-1	pancreas:	n/a
34	chr11:67577512-67577562	T-47D	breast:	n/a
35	chr11:67719813-67719863	AG04450	lung:	fetal
36	chr11:67572714-67572764	HRCEpiC	kidney:	n/a
37	chr11:67572714-67572764	HIPEpiC	eye:	n/a
38	chr11:67722909-67722959	SK-N-SH_RA	brain:	n/a
39	chr11:67746316-67746366	HRCEpiC	kidney:	n/a
40	chr11:67746316-67746366	AG04450	lung:	fetal
41	chr11:67723945-67723995	GM12892	blood:	n/a
42	chr11:67574013-67574063	AG10803	skin:	n/a
43	chr11:67572988-67573038	H1-hESC	embryonic stem cell:	embryo
44	chr11:67572716-67572766	AG04449	skin:	fetal
45	chr11:67746316-67746366	ProgFib	skin:	n/a
46	chr11:67568593-67568643	H1-hESC	embryonic stem cell:	embryo
47	chr11:67653560-67653610	K562	blood:	n/a
48	chr11:67723945-67723995	HCPEpiC	choroid plexus:	n/a
49	chr11:67726637-67726687	HRPEpiC	eye:	n/a
50	chr11:67577512-67577562	AG09319	gingival:	n/a

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

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

(count:18 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000221553	TF binding region
OR7E1P	TF binding region
ENSG00000251637	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
ENSG00000255230	TF binding region
ENSG00000254850	TF binding region
ENSG00000221553	CpG island
OR7E1P	CpG island
ENSG00000251637	CpG island
ALG1L8P	CpG island
RNU6-46P	CpG island
RPS3AP40	CpG island
FAM86C2P	CpG island
ENSG00000254792	CpG island
ENSG00000254610	CpG island
ENSG00000255230	CpG island
ENSG00000254850	CpG island
ENSG00000158483	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000171084	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000074800	chromatin interactions
ADAM9	miRNA target sites
TMC7	miRNA target sites
TP53	miRNA target sites
KIF21B	miRNA target sites
ABTB1	miRNA target sites

Extended variants
information (count: 8697 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8697 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7929569	chr11:67550395-67550396	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34740815	chr11:67550431-67550432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77569676	chr11:67550433-67550434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544762488	chr11:67550572-67550573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551606278	chr11:67550580-67550581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530167448	chr11:67550600-67550601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548521027	chr11:67550644-67550645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7110694	chr11:67550650-67550651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs528013454	chr11:67550653-67550654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552443220	chr11:67550699-67550700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570959764	chr11:67550719-67550720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538253099	chr11:67550720-67550721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550511650	chr11:67550721-67550722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568876037	chr11:67550726-67550727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185327757	chr11:67550738-67550739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374505012	chr11:67550824-67550825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549644499	chr11:67550845-67550846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573055984	chr11:67550847-67550848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534119964	chr11:67550849-67550850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11227948	chr11:67550852-67550853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7126757	chr11:67550861-67550862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544626159	chr11:67550863-67550864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7126764	chr11:67550880-67550881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10896224	chr11:67550881-67550882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147627655	chr11:67550882-67550883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560563107	chr11:67550891-67550892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527876333	chr11:67550898-67550899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552308813	chr11:67550902-67550903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7126882	chr11:67550944-67550945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531852376	chr11:67550945-67550946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10896225	chr11:67550985-67550986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368843091	chr11:67550989-67550990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539117597	chr11:67551018-67551019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568811932	chr11:67551033-67551034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9735907	chr11:67551047-67551048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141163822	chr11:67551061-67551062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572949741	chr11:67551070-67551071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566716067	chr11:67551071-67551072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533979612	chr11:67551112-67551113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35744117	chr11:67551130-67551131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137986330	chr11:67551191-67551192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575672189	chr11:67551228-67551229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9735098	chr11:67551229-67551230	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs201774720	chr11:67551230-67551231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538122477	chr11:67551236-67551237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556317652	chr11:67551238-67551239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540093921	chr11:67551246-67551247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11600353	chr11:67551262-67551263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560218920	chr11:67551273-67551274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367923236	chr11:67551275-67551276	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67547800-67553000	Weak transcription	Stomach Mucosa	stomach
2	chr11:67548000-67559400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:67553000-67553800	Enhancers	Stomach Mucosa	stomach
4	chr11:67553800-67555200	Weak transcription	Stomach Mucosa	stomach
5	chr11:67555200-67556600	Enhancers	Stomach Mucosa	stomach
6	chr11:67555400-67555600	Enhancers	Fetal Muscle Leg	muscle
7	chr11:67555400-67556000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:67555400-67556000	Enhancers	Colonic Mucosa	Colon
9	chr11:67555400-67556000	Enhancers	Fetal Intestine Large	intestine
10	chr11:67555400-67556000	Enhancers	Gastric	stomach
11	chr11:67555400-67556000	Enhancers	K562	blood
12	chr11:67555400-67556200	Enhancers	Placenta	Placenta
13	chr11:67555400-67556600	Enhancers	Fetal Intestine Small	intestine
14	chr11:67555600-67555800	Enhancers	Fetal Stomach	stomach
15	chr11:67555600-67556000	Enhancers	Placenta Amnion	Placenta Amnion
16	chr11:67555600-67556000	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr11:67555600-67556000	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr11:67555600-67556000	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:67555600-67557400	Weak transcription	Fetal Muscle Leg	muscle
20	chr11:67555800-67556000	Enhancers	Fetal Muscle Trunk	muscle
21	chr11:67555800-67560000	Weak transcription	Fetal Stomach	stomach
22	chr11:67556000-67559400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:67556000-67559400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr11:67556000-67571800	Weak transcription	Fetal Intestine Large	intestine
25	chr11:67556000-67572400	Weak transcription	Gastric	stomach
26	chr11:67556000-67572400	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:67556200-67557600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr11:67556200-67558000	Weak transcription	Placenta	Placenta
29	chr11:67556600-67559400	Weak transcription	Stomach Mucosa	stomach
30	chr11:67556600-67563200	Weak transcription	Fetal Intestine Small	intestine
31	chr11:67557200-67572200	Weak transcription	Thymus	Thymus
32	chr11:67557400-67559600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:67557400-67561000	Enhancers	Fetal Muscle Leg	muscle
34	chr11:67557600-67558400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:67557600-67560400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:67557600-67561200	Enhancers	Fetal Muscle Trunk	muscle
37	chr11:67558000-67558200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:67558000-67558200	Enhancers	Ovary	ovary
39	chr11:67558000-67558400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:67558000-67558400	Enhancers	Placenta	Placenta
41	chr11:67558000-67564000	Enhancers	Fetal Thymus	thymus
42	chr11:67558200-67558400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:67558200-67558400	Enhancers	Fetal Brain Female	brain
44	chr11:67558200-67558600	Enhancers	Fetal Heart	heart
45	chr11:67558200-67572000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:67558200-67572400	Weak transcription	Ovary	ovary
47	chr11:67558400-67559200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:67558400-67559400	Weak transcription	Placenta	Placenta
49	chr11:67558400-67560000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:67558400-67560000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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