Variant report

Variant	nsv975952
Chromosome Location	chr11:77523566-77526029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:306)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:77525963-77526100	HepG2	liver:	n/a	n/a
2	CBX3	chr11:77525774-77526280	K562	blood:	n/a	chr11:77526233-77526244
3	CBX3	chr11:77525732-77526396	K562	blood:	n/a	chr11:77526233-77526244
4	CBX3	chr11:77525899-77526322	HCT-116	colon:	n/a	chr11:77526233-77526244
5	GTF2F1	chr11:77525990-77526296	Hela-S3	cervix:	n/a	n/a
6	HEY1	chr11:77524717-77524791	HepG2	liver:	n/a	n/a
7	HEY1	chr11:77524652-77524821	K562	blood:	n/a	n/a
8	JUND	chr11:77525264-77525448	HepG2	liver:	n/a	chr11:77525271-77525282
9	KAP1	chr11:77525826-77526857	K562	blood:	n/a	n/a
10	KAP1	chr11:77525919-77526218	U2OS	brain:	n/a	n/a
11	KAP1	chr11:77525816-77526373	HEK293	kidney:	n/a	n/a
12	MXI1	chr11:77524109-77524194	K562	blood:	n/a	n/a
13	POLR2A	chr11:77524674-77524808	A549	lung:	n/a	n/a
14	POLR2A	chr11:77524735-77524995	MCF-7	breast:	n/a	n/a
15	POLR2A	chr11:77524651-77524877	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr11:77526011-77526147	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr11:77524645-77524795	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr11:77524775-77524791	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:77524674-77524726	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:77524688-77524851	MCF-7	breast:	n/a	n/a
21	POLR2A	chr11:77524611-77524913	GM12878	blood:	n/a	n/a
22	POLR2A	chr11:77524737-77524773	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr11:77524542-77524858	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr11:77524689-77524879	MCF-7	breast:	n/a	n/a
25	SETDB1	chr11:77525832-77526421	U2OS	brain:	n/a	n/a
26	SPI1	chr11:77525982-77526243	K562	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
27	SPI1	chr11:77525969-77526236	GM12891	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
28	SPI1	chr11:77526011-77526220	K562	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
29	SPI1	chr11:77525925-77526335	HL-60	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
30	SPI1	chr11:77525970-77526265	GM12891	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
31	SPI1	chr11:77525947-77526347	HL-60	blood:	n/a	chr11:77526124-77526137 chr11:77526125-77526138 chr11:77526130-77526143 chr11:77526127-77526136
32	TRIM28	chr11:77525801-77526386	K562	blood:	n/a	n/a
33	TRIM28	chr11:77525882-77526257	K562	blood:	n/a	n/a
34	USF1	chr11:77525947-77526208	K562	blood:	n/a	n/a
35	WRNIP1	chr11:77524558-77524707	GM12878	blood:	n/a	n/a
36	WRNIP1	chr11:77526012-77526254	GM12878	blood:	n/a	n/a
37	ZNF143	chr11:77525990-77526219	Hela-S3	cervix:	n/a	n/a
38	ZNF143	chr11:77525976-77526194	GM12878	blood:	n/a	n/a
39	ZNF143	chr11:77525953-77526289	H1-hESC	embryonic stem cell:	n/a	n/a
40	ZNF143	chr11:77525930-77526281	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:77524704-77524754	K562	blood:	n/a
2	chr11:77524704-77524754	K562	blood:	n/a
3	chr11:77524810-77524860	HNPCEpiC	eye:	n/a
4	chr11:77525780-77525830	HepG2	liver:	n/a
5	chr11:77524648-77524698	NT2-D1	testis:	n/a
6	chr11:77524648-77524698	IMR90	lung:	fetal
7	chr11:77524648-77524698	AG10803	skin:	n/a
8	chr11:77524648-77524698	HCT-116	colon:	n/a
9	chr11:77524766-77524816	NH-A	brain:	n/a
10	chr11:77524766-77524816	HEEpiC	esophagus:	n/a
11	chr11:77524766-77524816	HL-60	blood:	n/a
12	chr11:77525780-77525830	HCM	heart:	n/a
13	chr11:77525780-77525830	NH-A	brain:	n/a
14	chr11:77524648-77524698	GM06990	blood:	n/a
15	chr11:77524766-77524816	NHBE	bronchial:	n/a
16	chr11:77524648-77524698	NB4	blood:	n/a
17	chr11:77524704-77524754	U87	brain:	n/a
18	chr11:77525780-77525830	SK-N-MC	brain:	n/a
19	chr11:77524704-77524754	HNPCEpiC	eye:	n/a
20	chr11:77524810-77524860	U87	brain:	n/a
21	chr11:77524648-77524698	BE2_C	brain:	n/a
22	chr11:77524704-77524754	AG09309	skin:	n/a
23	chr11:77524766-77524816	GM12891	blood:	n/a
24	chr11:77524704-77524754	SK-N-MC	brain:	n/a
25	chr11:77524766-77524816	MCF-7	breast:	n/a
26	chr11:77524810-77524860	T-47D	breast:	n/a
27	chr11:77524810-77524860	AG09319	gingival:	n/a
28	chr11:77524704-77524754	BJ	skin:	n/a
29	chr11:77524704-77524754	Hepatocyte	liver:	n/a
30	chr11:77524648-77524698	PrEC	prostate:	n/a
31	chr11:77524810-77524860	NB4	blood:	n/a
32	chr11:77524704-77524754	HEEpiC	esophagus:	n/a
33	chr11:77524810-77524860	SK-N-MC	brain:	n/a
34	chr11:77524766-77524816	GM06990	blood:	n/a
35	chr11:77524704-77524754	GM12891	blood:	n/a
36	chr11:77524704-77524754	HMEC	breast:	n/a
37	chr11:77524648-77524698	GM12878	blood:	n/a
38	chr11:77524704-77524754	AoSMC	blood vessel:	n/a
39	chr11:77524648-77524698	HRE	kidney:	n/a
40	chr11:77524648-77524698	GM12892	blood:	n/a
41	chr11:77524766-77524816	K562	blood:	n/a
42	chr11:77524810-77524860	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:77524810-77524860	NHDF-neo	bronchial:	n/a
44	chr11:77524766-77524816	ECC-1	luminal epithelium:	n/a
45	chr11:77525780-77525830	NB4	blood:	n/a
46	chr11:77524810-77524860	K562	blood:	n/a
47	chr11:77525780-77525830	SAEC	small airway:	n/a
48	chr11:77524766-77524816	HUVEC	blood vessel:	n/a
49	chr11:77524704-77524754	AG09319	gingival:	n/a
50	chr11:77524648-77524698	HCPEpiC	choroid plexus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:77523579..77527566-chr11:77528400..77532529,6	K562	blood:
2	chr11:77521920..77524304-chr11:77525173..77528253,3	MCF-7	breast:
3	chr11:77521920..77524304-chr11:77525173..77528253,3	MCF-7	breast:
4	chr11:77520152..77525474-chr11:77528362..77532820,9	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS4-4	chr11:77524365-77524722	NONHSAT023232

No data

Variant related genes	Relation type
ENSG00000219529	TF binding region
ENSG00000219529	CpG island
ENSG00000048649	chromatin interactions
ENSG00000087884	chromatin interactions

Extended variants
information (count: 123 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:123 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532385850	chr11:77523588-77523589	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540862238	chr11:77523613-77523614	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559903275	chr11:77523714-77523715	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532402300	chr11:77523728-77523729	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs192404228	chr11:77523736-77523737	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77828179	chr11:77523780-77523781	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs527953847	chr11:77523793-77523794	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149331797	chr11:77523797-77523798	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551084817	chr11:77523865-77523866	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138083506	chr11:77523931-77523932	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs71046910	chr11:77523950-77523951	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185420695	chr11:77523995-77523996	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536349018	chr11:77524002-77524003	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546930307	chr11:77524034-77524035	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs566765273	chr11:77524043-77524044	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538927236	chr11:77524066-77524067	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189940801	chr11:77524136-77524137	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374093021	chr11:77524153-77524154	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575426583	chr11:77524185-77524186	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538097478	chr11:77524203-77524204	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554869578	chr11:77524217-77524218	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146264595	chr11:77524228-77524229	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529716571	chr11:77524241-77524242	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539968097	chr11:77524285-77524286	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs76238285	chr11:77524330-77524331	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs74439735	chr11:77524332-77524333	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs112615440	chr11:77524351-77524352	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576942735	chr11:77524371-77524372	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs181588557	chr11:77524395-77524396	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs547802720	chr11:77524406-77524407	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs186154299	chr11:77524428-77524429	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs562811096	chr11:77524445-77524446	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs569274272	chr11:77524447-77524448	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs548356400	chr11:77524465-77524466	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs561740448	chr11:77524515-77524516	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs531119843	chr11:77524560-77524561	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs530171782	chr11:77524563-77524564	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs546798129	chr11:77524631-77524632	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs374849813	chr11:77524638-77524639	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs552788238	chr11:77524640-77524641	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs188312822	chr11:77524644-77524645	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs180748415	chr11:77524648-77524649	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs569163515	chr11:77524651-77524652	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs186515835	chr11:77524663-77524664	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs117568957	chr11:77524668-77524669	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs191155383	chr11:77524693-77524694	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs533864119	chr11:77524705-77524706	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs58914857	chr11:77524722-77524723	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs576897702	chr11:77524732-77524733	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs374509065	chr11:77524734-77524735	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	20932292	CNVD
Cancer	20164920	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17142309	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77463800-77527000	Weak transcription	Aorta	Aorta
2	chr11:77475200-77527800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr11:77475400-77529000	Weak transcription	NHLF	lung
4	chr11:77475400-77530000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:77482800-77525800	Weak transcription	Fetal Lung	lung
6	chr11:77495800-77528200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr11:77496000-77530200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:77499000-77525600	Weak transcription	HMEC	breast
9	chr11:77501200-77525800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:77501400-77526800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr11:77503400-77525800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:77503600-77525000	Weak transcription	Ovary	ovary
13	chr11:77503600-77529600	Weak transcription	Right Ventricle	heart
14	chr11:77503800-77525800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr11:77504000-77524400	Weak transcription	Fetal Muscle Trunk	muscle
16	chr11:77504800-77524600	Weak transcription	Fetal Intestine Large	intestine
17	chr11:77504800-77525200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr11:77505000-77524000	Weak transcription	Fetal Muscle Leg	muscle
19	chr11:77505000-77528400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr11:77505200-77524200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr11:77505400-77525800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr11:77506800-77528200	Weak transcription	Brain Hippocampus Middle	brain
23	chr11:77508000-77527800	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:77509400-77528800	Weak transcription	Brain Germinal Matrix	brain
25	chr11:77509800-77530000	Weak transcription	NH-A	brain
26	chr11:77510000-77524600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:77511400-77526000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:77512000-77524800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:77512000-77525800	Weak transcription	NHDF-Ad	bronchial
30	chr11:77512000-77529600	Weak transcription	Stomach Smooth Muscle	stomach
31	chr11:77512200-77529200	Weak transcription	Fetal Brain Female	brain
32	chr11:77512400-77525400	Weak transcription	Psoas Muscle	Psoas
33	chr11:77512400-77530200	Weak transcription	Esophagus	oesophagus
34	chr11:77512400-77530600	Weak transcription	Lung	lung
35	chr11:77512600-77527000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr11:77512600-77530600	Weak transcription	Spleen	Spleen
37	chr11:77512800-77529800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr11:77512800-77530400	Weak transcription	Gastric	stomach
39	chr11:77513200-77529400	Weak transcription	Small Intestine	intestine
40	chr11:77514400-77526000	Weak transcription	NHEK	skin
41	chr11:77515400-77524600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:77515400-77530000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:77515600-77524400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:77516600-77530200	Weak transcription	HSMM	muscle
45	chr11:77517200-77529200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:77518400-77527000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr11:77518400-77528400	Weak transcription	Osteobl	bone
48	chr11:77518400-77529200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr11:77518600-77525400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr11:77518600-77525800	Weak transcription	Duodenum Smooth Muscle	Duodenum

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