Variant report

Variant	nsv897491
Chromosome Location	chr11:49498923-50058422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:50017185-50017430	HepG2	liver:	n/a	n/a
2	BACH1	chr11:49963039-49963171	K562	blood:	n/a	n/a
3	BACH1	chr11:49714575-49714772	K562	blood:	n/a	n/a
4	BATF	chr11:49851774-49851972	GM12878	blood:	n/a	n/a
5	BATF	chr11:49844388-49844674	GM12878	blood:	n/a	chr11:49844482-49844492
6	BATF	chr11:49900778-49901111	GM12878	blood:	n/a	n/a
7	BATF	chr11:49851722-49851990	GM12878	blood:	n/a	n/a
8	BATF	chr11:49878914-49879252	GM12878	blood:	n/a	n/a
9	BATF	chr11:49900767-49901127	GM12878	blood:	n/a	n/a
10	BATF	chr11:49908260-49908470	GM12878	blood:	n/a	n/a
11	BATF	chr11:49908186-49908527	GM12878	blood:	n/a	chr11:49908477-49908487
12	BATF	chr11:49844365-49844744	GM12878	blood:	n/a	chr11:49844482-49844492
13	BATF	chr11:49878972-49879182	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:49844437-49844676	GM12878	blood:	n/a	n/a
15	BCL11A	chr11:49908148-49908469	GM12878	blood:	n/a	n/a
16	BCL11A	chr11:49851712-49851919	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:50017239-50017377	K562	blood:	n/a	n/a
18	CBX3	chr11:50017099-50017442	K562	blood:	n/a	n/a
19	CBX3	chr11:50017158-50017392	K562	blood:	n/a	n/a
20	CEBPB	chr11:49945528-49945837	HepG2	liver:	n/a	chr11:49945657-49945666 chr11:49945657-49945666 chr11:49945657-49945666 chr11:49945657-49945668 chr11:49945655-49945668 chr11:49945655-49945666 chr11:49945657-49945666
21	CEBPB	chr11:49539391-49539648	IMR90	lung:	n/a	chr11:49539560-49539571
22	CEBPB	chr11:49795006-49795236	HepG2	liver:	n/a	chr11:49795070-49795079 chr11:49795068-49795079 chr11:49795170-49795181 chr11:49795170-49795181
23	CEBPB	chr11:49615707-49615848	HepG2	liver:	n/a	chr11:49615780-49615791 chr11:49615782-49615791 chr11:49615781-49615792 chr11:49615780-49615793
24	CEBPB	chr11:49795019-49795235	A549	lung:	n/a	chr11:49795070-49795079 chr11:49795068-49795079 chr11:49795170-49795181 chr11:49795170-49795181
25	CEBPB	chr11:49627245-49627460	A549	lung:	n/a	chr11:49627349-49627360 chr11:49627349-49627362
26	CEBPB	chr11:49633957-49634229	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:50047487-50047664	A549	lung:	n/a	n/a
28	CEBPB	chr11:49627187-49627468	HepG2	liver:	n/a	chr11:49627349-49627360 chr11:49627349-49627362
29	CEBPB	chr11:49794955-49795202	IMR90	lung:	n/a	chr11:49795070-49795079 chr11:49795068-49795079 chr11:49795170-49795181 chr11:49795170-49795181
30	CEBPB	chr11:49821217-49821358	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:49856098-49856319	HepG2	liver:	n/a	chr11:49856132-49856143
32	CEBPB	chr11:49782954-49783111	HepG2	liver:	n/a	chr11:49782976-49782987
33	CEBPB	chr11:49717874-49718074	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:49795023-49795152	Hela-S3	cervix:	n/a	chr11:49795070-49795079 chr11:49795068-49795079
35	CEBPB	chr11:49539385-49539635	HepG2	liver:	n/a	chr11:49539560-49539571
36	CEBPB	chr11:49856090-49856321	IMR90	lung:	n/a	chr11:49856132-49856143
37	CEBPB	chr11:49982821-49983021	HepG2	liver:	n/a	chr11:49982866-49982877
38	CEBPB	chr11:49709885-49710073	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:49856078-49856257	A549	lung:	n/a	chr11:49856132-49856143
40	CEBPB	chr11:49502468-49502676	A549	lung:	n/a	n/a
41	CEBPB	chr11:50056041-50056226	HepG2	liver:	n/a	chr11:50056106-50056117
42	CEBPB	chr11:49509838-49510050	HepG2	liver:	n/a	chr11:49509962-49509973
43	CEBPB	chr11:49945526-49945816	IMR90	lung:	n/a	chr11:49945657-49945666 chr11:49945657-49945666 chr11:49945657-49945666 chr11:49945657-49945668 chr11:49945655-49945668 chr11:49945655-49945666 chr11:49945657-49945666
44	CEBPB	chr11:49884315-49884602	HepG2	liver:	n/a	chr11:49884464-49884475
45	CHD2	chr11:50017167-50017356	K562	blood:	n/a	n/a
46	CTCF	chr11:50017220-50017370	GM12875	blood:	n/a	n/a
47	CTCF	chr11:49547840-49547990	GM12864	blood:	n/a	n/a
48	CTCF	chr11:49959749-49959812	LNCaP	prostate:	n/a	n/a
49	CTCF	chr11:49547960-49548110	HBMEC	blood vessel:	n/a	chr11:49547983-49548004 chr11:49547988-49548006
50	CTCF	chr11:49714167-49714282	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:49872191-49872241	AG09319	gingival:	n/a
2	chr11:49873118-49873168	CMK	blood:	n/a
3	chr11:49913868-49913918	PrEC	prostate:	n/a
4	chr11:49837274-49837324	HAEpiC	amniotic membrane:	n/a
5	chr11:49579457-49579507	HCPEpiC	choroid plexus:	n/a
6	chr11:49839512-49839562	NB4	blood:	n/a
7	chr11:49583127-49583177	HCPEpiC	choroid plexus:	n/a
8	chr11:49872191-49872241	AG09319	gingival:	n/a
9	chr11:49873118-49873168	CMK	blood:	n/a
10	chr11:49913868-49913918	PrEC	prostate:	n/a
11	chr11:49837274-49837324	HAEpiC	amniotic membrane:	n/a
12	chr11:49579457-49579507	HCPEpiC	choroid plexus:	n/a
13	chr11:49839512-49839562	NB4	blood:	n/a
14	chr11:49583127-49583177	HCPEpiC	choroid plexus:	n/a
15	chr11:49872169-49872219	AG04449	skin:	fetal
16	chr11:49843431-49843481	SK-N-SH_RA	brain:	n/a
17	chr11:49839281-49839331	H1-hESC	embryonic stem cell:	embryo
18	chr11:49582872-49582922	HEEpiC	esophagus:	n/a
19	chr11:49579997-49580047	HEK293	kidney:	embryo
20	chr11:49582872-49582922	NH-A	brain:	n/a
21	chr11:49802535-49802585	NHDF-neo	bronchial:	n/a
22	chr11:49582375-49582425	IMR90	lung:	fetal
23	chr11:49877977-49878027	GM06990	blood:	n/a
24	chr11:49913868-49913918	HepG2	liver:	n/a
25	chr11:49839281-49839331	HepG2	liver:	n/a
26	chr11:49580017-49580067	SK-N-SH_RA	brain:	n/a
27	chr11:49913230-49913280	HL-60	blood:	n/a
28	chr11:50003963-50004013	ECC-1	luminal epithelium:	n/a
29	chr11:49873118-49873168	Hepatocyte	liver:	n/a
30	chr11:50003963-50004013	LNCaP	prostate:	n/a
31	chr11:49580310-49580360	HRE	kidney:	n/a
32	chr11:49913868-49913918	SK-N-SH	brain:	n/a
33	chr11:49909689-49909739	HAEpiC	amniotic membrane:	n/a
34	chr11:49579457-49579507	GM19239	blood:	n/a
35	chr11:49877977-49878027	HAEpiC	amniotic membrane:	n/a
36	chr11:49873813-49873863	HRPEpiC	eye:	n/a
37	chr11:49582872-49582922	GM12892	blood:	n/a
38	chr11:49839512-49839562	GM12892	blood:	n/a
39	chr11:50004210-50004260	Jurkat	blood:	n/a
40	chr11:50004210-50004260	ovcar-3	ovarian:	n/a
41	chr11:49911386-49911436	SK-N-SH	brain:	n/a
42	chr11:49872191-49872241	U87	brain:	n/a
43	chr11:49909689-49909739	BE2_C	brain:	n/a
44	chr11:49875844-49875894	AG04449	skin:	fetal
45	chr11:49917069-49917119	Hepatocyte	liver:	n/a
46	chr11:49917865-49917915	HUVEC	blood vessel:	n/a
47	chr11:50003963-50004013	H1-hESC	embryonic stem cell:	embryo
48	chr11:49873682-49873732	U87	brain:	n/a
49	chr11:49839836-49839886	HUVEC	blood vessel:	n/a
50	chr11:49839281-49839331	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:49547545..49548055-chr11:50016701..50017446,2	MCF-7	breast:
2	chr11:17658237..17658957-chr11:49872663..49873515,2	MCF-7	breast:
3	chr11:49917687..49918187-chr7:157901646..157902182,2	MCF-7	breast:
4	chr11:49547545..49548055-chr11:50016701..50017446,2	MCF-7	breast:
5	chr11:49250422..49251012-chr11:49547571..49548253,2	MCF-7	breast:
6	chr11:49251863..49252437-chr11:49547367..49548407,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C12-7	chr11:49880918-49880954	NONHSAT021319
2	lnc-OR4C12-7	chr11:49879271-49879391	NONHSAT021319
3	lnc-OR4C13-4	chr11:49896497-49896595	NONHSAT021320
4	lnc-OR4C12-7	chr11:49876073-49876325	NONHSAT021319
5	lnc-OR4C12-7	chr11:49875632-49875959	NONHSAT021319
6	lnc-OR4C13-3	chr11:49905555-49905645	NONHSAT021321
7	lnc-OR4C13-3	chr11:49904551-49904952	NONHSAT021321
8	lnc-OR4C13-4	chr11:49897694-49898190	NONHSAT021320

Variant related genes	Relation type
TRIM51DP	TF binding region
ENSG00000254487	TF binding region
OR4A1P	TF binding region
TRIM51FP	TF binding region
ENSG00000255268	TF binding region
ENSG00000255111	TF binding region
ENSG00000254714	TF binding region
OR4A49P	TF binding region
ENSG00000254800	TF binding region
OR4A19P	TF binding region
ENSG00000205035	TF binding region
OR4A18P	TF binding region
ENSG00000255214	TF binding region
ENSG00000255550	TF binding region
OR4C12	TF binding region
OR4C13	TF binding region
OR4R3P	TF binding region
TRIM51DP	CpG island
ENSG00000254487	CpG island
OR4A1P	CpG island
TRIM51FP	CpG island
ENSG00000255268	CpG island
ENSG00000255111	CpG island
ENSG00000254714	CpG island
OR4A49P	CpG island
ENSG00000254800	CpG island
OR4A19P	CpG island
ENSG00000205035	CpG island
OR4A18P	CpG island
ENSG00000255214	CpG island
ENSG00000255550	CpG island
OR4C12	CpG island
OR4C13	CpG island
OR4R3P	CpG island

Extended variants
information (count: 2514 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2514 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548643587	chr11:49526401-49526402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560148624	chr11:49526491-49526492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544589031	chr11:49526498-49526499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116552917	chr11:49526563-49526564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530309997	chr11:49526566-49526567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540450272	chr11:49526594-49526595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7107178	chr11:49526668-49526669	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532090222	chr11:49526722-49526723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573263749	chr11:49526742-49526743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373874707	chr11:49526745-49526746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552106184	chr11:49526751-49526752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs16914192	chr11:49526801-49526802	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs568931482	chr11:49526818-49526819	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181939122	chr11:49526861-49526862	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548154473	chr11:49526902-49526903	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568291606	chr11:49526947-49526948	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs534051299	chr11:49526978-49526979	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs554024234	chr11:49527045-49527046	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs138458504	chr11:49527075-49527076	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10839294	chr11:49527076-49527077	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs115251079	chr11:49527077-49527078	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs200582336	chr11:49527079-49527080	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200945499	chr11:49527088-49527089	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs34529813	chr11:49527089-49527090	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs575682689	chr11:49527100-49527101	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs186087252	chr11:49527125-49527126	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570423526	chr11:49527132-49527133	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201715331	chr11:49527155-49527156	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs574810739	chr11:49527221-49527222	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs190951775	chr11:49527235-49527236	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs560316306	chr11:49527263-49527264	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs140187746	chr11:49527272-49527273	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs559891978	chr11:49527308-49527309	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs542919574	chr11:49527330-49527331	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs10839295	chr11:49527345-49527346	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs2866575	chr11:49544211-49544212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577449343	chr11:49544216-49544217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2866576	chr11:49544237-49544238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141912259	chr11:49544252-49544253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562663898	chr11:49544273-49544274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531658449	chr11:49544274-49544275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542215194	chr11:49544281-49544282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2866577	chr11:49544288-49544289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2866578	chr11:49544289-49544290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2866579	chr11:49544295-49544296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2866580	chr11:49544326-49544327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185827472	chr11:49544391-49544392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534595044	chr11:49545007-49545008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34684910	chr11:49545056-49545057	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577486211	chr11:49545165-49545166	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Autism	22495309	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:49526400-49526800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr11:49526400-49526800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr11:49526600-49527400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr11:49526800-49527200	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr11:49527000-49527400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr11:49527000-49527400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr11:49527200-49527400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:49544200-49544400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:49545000-49545200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:49551400-49552200	Enhancers	Liver	Liver
11	chr11:49579200-49581200	Active TSS	Brain Anterior Caudate	brain
12	chr11:49579800-49580000	Bivalent Enhancer	Brain Germinal Matrix	brain
13	chr11:49579800-49580200	Active TSS	Brain Cingulate Gyrus	brain
14	chr11:49579800-49580200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
15	chr11:49579800-49580200	Enhancers	Pancreas	Pancrea
16	chr11:49579800-49580400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr11:49579800-49580400	Bivalent/Poised TSS	Fetal Brain Female	brain
18	chr11:49579800-49580600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:49579800-49581200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr11:49579800-49581200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:49579800-49581400	Active TSS	Brain Angular Gyrus	brain
22	chr11:49580000-49580400	Active TSS	Brain Germinal Matrix	brain
23	chr11:49580200-49580400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
24	chr11:49580200-49580400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
25	chr11:49580200-49580600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr11:49580400-49580600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
27	chr11:49580600-49580800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:49580600-49580800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
29	chr11:49581200-49581400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
30	chr11:49581200-49581400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:49581200-49582200	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr11:49581400-49582400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr11:49581400-49582800	Weak transcription	Brain Angular Gyrus	brain
34	chr11:49582200-49582400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
35	chr11:49582200-49584400	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr11:49582400-49582600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:49582400-49582600	Enhancers	Fetal Brain Female	brain
38	chr11:49582400-49583400	Active TSS	Brain Hippocampus Middle	brain
39	chr11:49582400-49584400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:49582600-49582800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:49582600-49583200	Active TSS	Fetal Brain Female	brain
42	chr11:49582800-49583200	Active TSS	Brain Germinal Matrix	brain
43	chr11:49582800-49583600	Active TSS	Brain Cingulate Gyrus	brain
44	chr11:49582800-49584400	Active TSS	Brain Angular Gyrus	brain
45	chr11:49582800-49584400	Active TSS	Brain Anterior Caudate	brain
46	chr11:49660800-49661200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr11:49695200-49695400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:49696200-49696800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
49	chr11:49699000-49699400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:49699000-49699400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast

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