Variant report

Variant	nsv7693
Chromosome Location	chr11:17556788-17601771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:1586)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:17572084-17572296	K562	blood:	n/a	n/a
2	BACH1	chr11:17566012-17566149	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:17597341-17597624	K562	blood:	n/a	chr11:17597468-17597477
4	BHLHE40	chr11:17597349-17597729	HepG2	liver:	n/a	chr11:17597468-17597477
5	CCNT2	chr11:17593825-17594070	K562	blood:	n/a	n/a
6	CEBPB	chr11:17561324-17561348	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr11:17588780-17589028	HepG2	liver:	n/a	chr11:17588880-17588889 chr11:17588878-17588889
8	CEBPB	chr11:17568597-17569010	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr11:17569793-17569873	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr11:17584988-17585129	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr11:17563107-17563184	HepG2	liver:	n/a	n/a
12	CTCF	chr11:17570020-17570170	BJ	skin:	n/a	n/a
13	CTCF	chr11:17586360-17586510	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr11:17586320-17586470	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr11:17570140-17570290	HCT-116	colon:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
16	CTCF	chr11:17586360-17586510	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr11:17586263-17586499	GM12878	blood:	n/a	n/a
18	CTCF	chr11:17586113-17586584	K562	blood:	n/a	n/a
19	CTCF	chr11:17585094-17585164	GM12892	blood:	n/a	n/a
20	CTCF	chr11:17586336-17586466	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:17570100-17570250	HMEC	breast:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
22	CTCF	chr11:17570100-17570250	HCM	heart:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
23	CTCF	chr11:17570000-17570150	GM12864	blood:	n/a	n/a
24	CTCF	chr11:17570140-17570290	HRE	kidney:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
25	CTCF	chr11:17570162-17570249	HepG2	liver:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
26	CTCF	chr11:17560293-17560624	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr11:17576040-17576190	GM12870	blood:	n/a	n/a
28	CTCF	chr11:17576164-17576235	K562	blood:	n/a	n/a
29	CTCF	chr11:17586340-17586490	HRE	kidney:	n/a	n/a
30	CTCF	chr11:17569560-17569710	Caco-2	colon:	n/a	n/a
31	CTCF	chr11:17560400-17560550	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr11:17584960-17585110	HepG2	liver:	n/a	n/a
33	CTCF	chr11:17584900-17585050	GM12867	blood:	n/a	n/a
34	CTCF	chr11:17570080-17570230	HEEpiC	esophagus:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
35	CTCF	chr11:17575920-17576070	HCT-116	colon:	n/a	chr11:17576037-17576055
36	CTCF	chr11:17576100-17576250	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr11:17570080-17570230	GM12869	blood:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
38	CTCF	chr11:17560374-17560539	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:17576180-17576330	GM12875	blood:	n/a	n/a
40	CTCF	chr11:17569640-17569790	RPTEC	kidney:	n/a	n/a
41	CTCF	chr11:17586323-17586486	GM10266	blood:	n/a	n/a
42	CTCF	chr11:17570145-17570242	A549	lung:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
43	CTCF	chr11:17576100-17576250	HepG2	liver:	n/a	n/a
44	CTCF	chr11:17598680-17598830	GM12869	blood:	n/a	n/a
45	CTCF	chr11:17586340-17586490	BJ	skin:	n/a	n/a
46	CTCF	chr11:17585060-17585210	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr11:17586340-17586490	HEK293	kidney:	n/a	n/a
48	CTCF	chr11:17576120-17576270	HEK293	kidney:	n/a	n/a
49	CTCF	chr11:17570062-17570251	K562	blood:	n/a	chr11:17570198-17570208 chr11:17570201-17570210
50	CTCF	chr11:17569580-17569730	HBMEC	blood vessel:	n/a	n/a

(count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17598735-17598785	HRE	kidney:	n/a
2	chr11:17566011-17566061	SK-N-SH_RA	brain:	n/a
3	chr11:17564425-17564475	AoSMC	blood vessel:	n/a
4	chr11:17568889-17568939	HRPEpiC	eye:	n/a
5	chr11:17591822-17591872	T-47D	breast:	n/a
6	chr11:17598735-17598785	A549	lung:	n/a
7	chr11:17563125-17563175	PFSK-1	brain:	n/a
8	chr11:17566011-17566061	T-47D	breast:	n/a
9	chr11:17591873-17591923	NB4	blood:	n/a
10	chr11:17566051-17566101	NT2-D1	testis:	n/a
11	chr11:17565769-17565819	SK-N-SH	brain:	n/a
12	chr11:17564696-17564746	AG10803	skin:	n/a
13	chr11:17567447-17567497	PANC-1	pancreas:	n/a
14	chr11:17566011-17566061	SK-N-MC	brain:	n/a
15	chr11:17599798-17599848	HCPEpiC	choroid plexus:	n/a
16	chr11:17565744-17565794	HMEC	breast:	n/a
17	chr11:17565885-17565935	PANC-1	pancreas:	n/a
18	chr11:17563125-17563175	Jurkat	blood:	n/a
19	chr11:17591822-17591872	HRCEpiC	kidney:	n/a
20	chr11:17567447-17567497	GM12878	blood:	n/a
21	chr11:17599715-17599765	AG04450	lung:	fetal
22	chr11:17566163-17566213	AoSMC	blood vessel:	n/a
23	chr11:17599691-17599741	HRE	kidney:	n/a
24	chr11:17569556-17569606	Hela-S3	cervix:	n/a
25	chr11:17599691-17599741	AG09309	skin:	n/a
26	chr11:17591822-17591872	ProgFib	skin:	n/a
27	chr11:17566034-17566084	Hepatocyte	liver:	n/a
28	chr11:17598735-17598785	SAEC	small airway:	n/a
29	chr11:17591873-17591923	HCPEpiC	choroid plexus:	n/a
30	chr11:17568889-17568939	HEK293	kidney:	embryo
31	chr11:17565744-17565794	NB4	blood:	n/a
32	chr11:17599798-17599848	NB4	blood:	n/a
33	chr11:17599798-17599848	BJ	skin:	n/a
34	chr11:17599691-17599741	GM12891	blood:	n/a
35	chr11:17569556-17569606	ProgFib	skin:	n/a
36	chr11:17566051-17566101	RPTEC	kidney:	n/a
37	chr11:17566048-17566098	U87	brain:	n/a
38	chr11:17591822-17591872	CMK	blood:	n/a
39	chr11:17566048-17566098	HL-60	blood:	n/a
40	chr11:17565744-17565794	T-47D	breast:	n/a
41	chr11:17565769-17565819	HEEpiC	esophagus:	n/a
42	chr11:17591822-17591872	A549	lung:	n/a
43	chr11:17568889-17568939	U87	brain:	n/a
44	chr11:17564425-17564475	RPTEC	kidney:	n/a
45	chr11:17599798-17599848	IMR90	lung:	fetal
46	chr11:17599365-17599415	SK-N-SH	brain:	n/a
47	chr11:17566034-17566084	ovcar-3	ovarian:	n/a
48	chr11:17599365-17599415	HCF	heart:	n/a
49	chr11:17565769-17565819	AG04449	skin:	fetal
50	chr11:17564696-17564746	GM12892	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17564338..17566127-chr11:17572702..17576571,3	K562	blood:
2	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
3	chr11:17558247..17559969-chr11:17568227..17570175,2	K562	blood:
4	chr11:17594662..17597692-chr11:17599938..17601708,3	K562	blood:
5	chr11:17563988..17566643-chr11:17568666..17571231,2	MCF-7	breast:
6	chr11:17594662..17597692-chr11:17599938..17601708,3	K562	blood:
7	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
8	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
9	chr11:17580038..17581891-chr11:17582778..17585148,2	K562	blood:
10	chr11:17573695..17575515-chr11:17575864..17578594,2	K562	blood:
11	chr11:17595636..17597692-chr11:17599938..17601981,3	K562	blood:
12	chr11:17584725..17586615-chr11:17597092..17599857,2	MCF-7	breast:
13	chr11:17557311..17560136-chr11:17561870..17563782,2	K562	blood:
14	chr11:17569821..17570438-chr11:17586271..17587120,2	MCF-7	breast:
15	chr11:17595636..17597692-chr11:17599938..17601981,3	K562	blood:
16	chr11:17567943..17569861-chr11:17577683..17579553,2	K562	blood:
17	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
18	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
19	chr11:17580038..17581891-chr11:17582778..17585148,2	K562	blood:
20	chr11:17567135..17572180-chr11:17576316..17581948,6	K562	blood:
21	chr11:17567562..17569215-chr11:17583534..17585455,2	K562	blood:
22	chr11:17550003..17552043-chr11:17563166..17565257,2	K562	blood:
23	chr11:17554291..17557125-chr11:17558715..17560348,2	MCF-7	breast:
24	chr11:17520408..17522288-chr11:17583277..17586222,2	K562	blood:
25	chr11:17563988..17566643-chr11:17568666..17571231,2	MCF-7	breast:
26	chr11:17579575..17581891-chr11:17582600..17585148,3	K562	blood:
27	chr11:17557311..17560136-chr11:17561870..17563782,2	K562	blood:
28	chr11:17597969..17599564-chr11:17601245..17604128,2	K562	blood:
29	chr11:17597969..17599564-chr11:17601245..17604128,2	K562	blood:
30	chr11:17567135..17572180-chr11:17576316..17581948,6	K562	blood:
31	chr11:17569821..17570438-chr11:17586271..17587120,2	MCF-7	breast:
32	chr11:17579575..17581891-chr11:17582600..17585148,3	K562	blood:

No data

Variant related genes	Relation type
OTOG	TF binding region
USH1C	TF binding region
OTOG	CpG island
USH1C	CpG island
ENSG00000006611	chromatin interactions
ENSG00000188162	chromatin interactions

Extended variants
information (count: 1881 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564789088	chr11:17556795-17556796	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532229297	chr11:17556817-17556818	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191851679	chr11:17556821-17556822	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139934808	chr11:17556871-17556872	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143679278	chr11:17556901-17556902	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs146806104	chr11:17556904-17556905	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs35176543	chr11:17556914-17556915	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs375380122	chr11:17556968-17556969	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182475182	chr11:17556969-17556970	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs187695180	chr11:17556982-17556983	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs558708576	chr11:17556994-17556995	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2237959	chr11:17557017-17557018	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs372644519	chr11:17557040-17557041	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539101761	chr11:17557093-17557094	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557112357	chr11:17557127-17557128	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs192761125	chr11:17557138-17557139	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377505920	chr11:17557174-17557175	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs534955642	chr11:17557185-17557186	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs542938203	chr11:17557261-17557262	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370382735	chr11:17557269-17557270	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148539520	chr11:17557278-17557279	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573113013	chr11:17557281-17557282	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556291852	chr11:17557357-17557358	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112652967	chr11:17557371-17557372	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142745695	chr11:17557455-17557456	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532139468	chr11:17557458-17557459	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112563315	chr11:17557478-17557479	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112220254	chr11:17557547-17557548	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs34723369	chr11:17557619-17557620	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs61880350	chr11:17557691-17557692	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs184138013	chr11:17557717-17557718	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535279456	chr11:17557720-17557721	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs112139323	chr11:17557811-17557812	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552116180	chr11:17557812-17557813	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151038960	chr11:17557843-17557844	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538772484	chr11:17557855-17557856	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369290402	chr11:17557865-17557866	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189062169	chr11:17557892-17557893	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78484388	chr11:17557906-17557907	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536206206	chr11:17557913-17557914	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377401242	chr11:17557920-17557921	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554535734	chr11:17558034-17558035	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543971701	chr11:17558050-17558051	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377736142	chr11:17558079-17558080	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573483651	chr11:17558108-17558109	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540904532	chr11:17558130-17558131	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554053695	chr11:17558165-17558166	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562276475	chr11:17558178-17558179	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192507890	chr11:17558185-17558186	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184682119	chr11:17558203-17558204	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17538400-17562200	Weak transcription	Small Intestine	intestine
2	chr11:17547200-17563200	Genic enhancers	Fetal Intestine Small	intestine
3	chr11:17553600-17557000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:17553600-17557200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:17553600-17561800	Weak transcription	Gastric	stomach
6	chr11:17553600-17562200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:17553800-17556800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr11:17553800-17558200	Weak transcription	Stomach Mucosa	stomach
9	chr11:17553800-17558600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr11:17553800-17563200	Weak transcription	Colonic Mucosa	Colon
11	chr11:17555400-17560400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr11:17555800-17562400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr11:17556000-17558000	Enhancers	Hela-S3	cervix
14	chr11:17556200-17556800	Weak transcription	Fetal Intestine Large	intestine
15	chr11:17556600-17557400	Enhancers	Brain Anterior Caudate	brain
16	chr11:17556800-17557400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr11:17556800-17557600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr11:17556800-17558800	Enhancers	Fetal Intestine Large	intestine
19	chr11:17557200-17557400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:17557200-17557800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr11:17557800-17558000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:17558000-17558400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:17558000-17563400	Weak transcription	Hela-S3	cervix
24	chr11:17558200-17559800	Enhancers	Stomach Mucosa	stomach
25	chr11:17558400-17563200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:17558600-17559000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr11:17558800-17562200	Genic enhancers	Fetal Intestine Large	intestine
28	chr11:17559000-17561800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr11:17559600-17560600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:17559800-17560200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:17559800-17562000	Weak transcription	Stomach Mucosa	stomach
32	chr11:17560200-17560600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr11:17560200-17562200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr11:17560400-17562600	Enhancers	Duodenum Mucosa	Duodenum
35	chr11:17560600-17560800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:17560800-17562000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:17561800-17562200	Enhancers	Gastric	stomach
38	chr11:17561800-17562800	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr11:17561800-17563000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr11:17562000-17564000	Enhancers	Stomach Mucosa	stomach
41	chr11:17562000-17565200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:17562200-17562400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:17562200-17562400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr11:17562200-17562400	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
45	chr11:17562200-17564400	Weak transcription	Gastric	stomach
46	chr11:17562400-17562600	Enhancers	Small Intestine	intestine
47	chr11:17562400-17562800	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr11:17562400-17564400	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr11:17562400-17566200	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr11:17562600-17562800	Flanking Active TSS	Duodenum Mucosa	Duodenum

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