Variant report

Variant	nsv832145
Chromosome Location	chr11:49002873-49185190
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	BRCA1	chr11:49169276-49169286	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr11:49176276-49176584	HepG2	liver:	n/a	chr11:49176450-49176463 chr11:49176420-49176429 chr11:49176418-49176429 chr11:49176450-49176461 chr11:49176420-49176431
3	CEBPB	chr11:49176297-49176560	IMR90	lung:	n/a	chr11:49176450-49176463 chr11:49176420-49176429 chr11:49176418-49176429 chr11:49176450-49176461 chr11:49176420-49176431
4	CEBPB	chr11:49026623-49026812	K562	blood:	n/a	chr11:49026677-49026686 chr11:49026675-49026688 chr11:49026677-49026686 chr11:49026677-49026686 chr11:49026675-49026686 chr11:49026677-49026688 chr11:49026728-49026739 chr11:49026677-49026686
5	CEBPB	chr11:49026617-49026956	Hela-S3	cervix:	n/a	chr11:49026677-49026686 chr11:49026675-49026688 chr11:49026677-49026686 chr11:49026677-49026686 chr11:49026675-49026686 chr11:49026677-49026688 chr11:49026728-49026739 chr11:49026677-49026686
6	CEBPB	chr11:49026601-49026811	HepG2	liver:	n/a	chr11:49026677-49026686 chr11:49026675-49026688 chr11:49026677-49026686 chr11:49026677-49026686 chr11:49026675-49026686 chr11:49026677-49026688 chr11:49026728-49026739 chr11:49026677-49026686
7	CEBPB	chr11:49131188-49131388	A549	lung:	n/a	n/a
8	CEBPB	chr11:49176304-49176533	A549	lung:	n/a	chr11:49176450-49176463 chr11:49176420-49176429 chr11:49176418-49176429 chr11:49176450-49176461 chr11:49176420-49176431
9	CTCF	chr11:49070401-49070689	K562	blood:	n/a	chr11:49070519-49070537 chr11:49070521-49070534 chr11:49070520-49070536 chr11:49070514-49070535 chr11:49070521-49070534
10	CTCF	chr11:49098521-49098572	GM13976	blood:	n/a	chr11:49098536-49098544
11	CTCF	chr11:49048063-49048097	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr11:49146614-49146686	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr11:49071985-49072040	LNCaP	prostate:	n/a	n/a
14	CTCF	chr11:49107115-49107175	GM10248	blood:	n/a	n/a
15	CTCF	chr11:49022831-49022955	GM20000	blood:	n/a	n/a
16	CTCF	chr11:49104077-49104129	GM10248	blood:	n/a	n/a
17	CTCF	chr11:49089926-49089944	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr11:49070476-49070576	K562	blood:	n/a	chr11:49070519-49070537 chr11:49070521-49070534 chr11:49070520-49070536 chr11:49070514-49070535 chr11:49070521-49070534
19	CTCF	chr11:49070398-49070685	K562	blood:	n/a	chr11:49070519-49070537 chr11:49070521-49070534 chr11:49070520-49070536 chr11:49070514-49070535 chr11:49070521-49070534
20	CTCF	chr11:49067670-49067676	GM13976	blood:	n/a	n/a
21	CTCF	chr11:49167369-49167420	GM20000	blood:	n/a	n/a
22	CTCF	chr11:49087338-49087430	Lung_OC	lung:	n/a	n/a
23	CTCF	chr11:49098901-49098918	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr11:49145521-49145567	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr11:49071340-49071490	HEK293	kidney:	n/a	n/a
26	CTCF	chr11:49092621-49092790	A549	lung:	n/a	chr11:49092683-49092701
27	CTCF	chr11:49067615-49067665	GM13976	blood:	n/a	n/a
28	CTCF	chr11:49067101-49067189	GM13977	blood:	n/a	n/a
29	CTCF	chr11:49152811-49152868	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr11:49127919-49127961	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:49053116-49053137	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:49050048-49050098	GM13976	blood:	n/a	n/a
33	CTCF	chr11:49048171-49048237	GM20000	blood:	n/a	n/a
34	CTCF	chr11:49104378-49104448	GM10266	blood:	n/a	n/a
35	CTCF	chr11:49092679-49092714	Medullo	brain:	n/a	chr11:49092683-49092701
36	CTCF	chr11:49130096-49130142	GM10248	blood:	n/a	n/a
37	CTCF	chr11:49052021-49052104	GM13976	blood:	n/a	n/a
38	CTCF	chr11:49071434-49071865	K562	blood:	n/a	n/a
39	CTCF	chr11:49027702-49027760	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr11:49106248-49106299	GM10266	blood:	n/a	n/a
41	CTCF	chr11:49080840-49080919	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr11:49061169-49061228	GM13977	blood:	n/a	n/a
43	CTCF	chr11:49067908-49067939	LNCaP	prostate:	n/a	n/a
44	CTCF	chr11:49180814-49180881	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr11:49071523-49071763	K562	blood:	n/a	n/a
46	CTCF	chr11:49085811-49085890	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr11:49100463-49100499	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr11:49004817-49004881	LNCaP	prostate:	n/a	n/a
49	CTCF	chr11:49070501-49070571	Pancreas_OC	pancreas:	n/a	chr11:49070519-49070537 chr11:49070521-49070534 chr11:49070520-49070536 chr11:49070514-49070535 chr11:49070521-49070534
50	CTCF	chr11:49023336-49023420	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:49081540-49081590	AG09309	skin:	n/a
2	chr11:49081540-49081590	SAEC	small airway:	n/a
3	chr11:49124111-49124161	PANC-1	pancreas:	n/a
4	chr11:49123325-49123375	Hepatocyte	liver:	n/a
5	chr11:49073835-49073885	HL-60	blood:	n/a
6	chr11:49081540-49081590	AG09309	skin:	n/a
7	chr11:49081540-49081590	SAEC	small airway:	n/a
8	chr11:49124111-49124161	PANC-1	pancreas:	n/a
9	chr11:49123325-49123375	Hepatocyte	liver:	n/a
10	chr11:49073835-49073885	HL-60	blood:	n/a
11	chr11:49124090-49124140	HIPEpiC	eye:	n/a
12	chr11:49123325-49123375	HCM	heart:	n/a
13	chr11:49123970-49124020	HCPEpiC	choroid plexus:	n/a
14	chr11:49072348-49072398	SK-N-MC	brain:	n/a
15	chr11:49123325-49123375	HRE	kidney:	n/a
16	chr11:49073835-49073885	PFSK-1	brain:	n/a
17	chr11:49071438-49071488	A549	lung:	n/a
18	chr11:49073835-49073885	SK-N-SH_RA	brain:	n/a
19	chr11:49123325-49123375	SK-N-SH_RA	brain:	n/a
20	chr11:49072348-49072398	NHBE	bronchial:	n/a
21	chr11:49124111-49124161	SK-N-SH_RA	brain:	n/a
22	chr11:49003527-49003577	HL-60	blood:	n/a
23	chr11:49003527-49003577	AG09309	skin:	n/a
24	chr11:49072348-49072398	HEK293	kidney:	embryo
25	chr11:49124090-49124140	ECC-1	luminal epithelium:	n/a
26	chr11:49124791-49124841	CMK	blood:	n/a
27	chr11:49017551-49017601	SKMC	muscle:	n/a
28	chr11:49017551-49017601	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:49003361-49003411	LNCaP	prostate:	n/a
30	chr11:49123970-49124020	GM12891	blood:	n/a
31	chr11:49070005-49070055	BE2_C	brain:	n/a
32	chr11:49003361-49003411	SK-N-SH	brain:	n/a
33	chr11:49070231-49070281	GM06990	blood:	n/a
34	chr11:49068653-49068703	HEK293	kidney:	embryo
35	chr11:49071763-49071813	Jurkat	blood:	n/a
36	chr11:49017551-49017601	SK-N-MC	brain:	n/a
37	chr11:49003361-49003411	ProgFib	skin:	n/a
38	chr11:49124111-49124161	HRPEpiC	eye:	n/a
39	chr11:49003361-49003411	HCT-116	colon:	n/a
40	chr11:49071438-49071488	HEK293	kidney:	embryo
41	chr11:49128127-49128177	H1-hESC	embryonic stem cell:	embryo
42	chr11:49070637-49070687	HEEpiC	esophagus:	n/a
43	chr11:49073835-49073885	HNPCEpiC	eye:	n/a
44	chr11:49070005-49070055	Jurkat	blood:	n/a
45	chr11:49049039-49049089	ProgFib	skin:	n/a
46	chr11:49070637-49070687	LNCaP	prostate:	n/a
47	chr11:49124090-49124140	NT2-D1	testis:	n/a
48	chr11:49070637-49070687	GM12892	blood:	n/a
49	chr11:49123325-49123375	Caco-2	colon:	n/a
50	chr11:49070231-49070281	HCT-116	colon:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-1	chr11:49113956-49114319	NONHSAT021308
2	lnc-TRIM64C-1	chr11:49092304-49092552	NONHSAT021307
3	lnc-AC084851.1-3	chr11:49132308-49132772	NONHSAT021309
4	lnc-FOLH1-1	chr11:49155205-49156352	NONHSAT021310

Variant related genes	Relation type
UBTFL7	TF binding region
ENSG00000205044	TF binding region
TRIM49B	TF binding region
TRIM53CP	TF binding region
ENSG00000254801	TF binding region
ENSG00000254567	TF binding region
FOLH1	TF binding region
TRIM51GP	TF binding region
TRIM64C	TF binding region
ENSG00000254412	TF binding region
ENSG00000254993	TF binding region
ENSG00000255452	TF binding region
ENSG00000255338	TF binding region
UBTFL7	CpG island
ENSG00000205044	CpG island
TRIM49B	CpG island
TRIM53CP	CpG island
ENSG00000254801	CpG island
ENSG00000254567	CpG island
FOLH1	CpG island
TRIM51GP	CpG island
TRIM64C	CpG island
ENSG00000254412	CpG island
ENSG00000254993	CpG island
ENSG00000255452	CpG island
ENSG00000255338	CpG island

Extended variants
information (count: 1159 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576649544	chr11:49003361-49003362	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs11608048	chr11:49003362-49003363	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192491541	chr11:49003377-49003378	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs572571059	chr11:49003385-49003386	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs533846941	chr11:49003397-49003398	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs541576755	chr11:49003407-49003408	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs551531892	chr11:49003527-49003528	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs571497116	chr11:49003540-49003541	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs376497992	chr11:49003548-49003549	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs572571881	chr11:49003549-49003550	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs189387935	chr11:49003555-49003556	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs557250890	chr11:49003565-49003566	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs59228939	chr11:49004830-49004831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189672785	chr11:49005280-49005281	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562372723	chr11:49007546-49007547	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs527323120	chr11:49007593-49007594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138021705	chr11:49007614-49007615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs575512435	chr11:49013517-49013518	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555667907	chr11:49013523-49013524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs553953534	chr11:49013532-49013533	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs540665894	chr11:49013559-49013560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs181630250	chr11:49013571-49013572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201728799	chr11:49013623-49013624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs79372372	chr11:49013637-49013638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs200997676	chr11:49013655-49013656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544539006	chr11:49013674-49013675	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs186765795	chr11:49013682-49013683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs1847643	chr11:49013685-49013686	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs190779541	chr11:49013700-49013701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147998527	chr11:49013701-49013702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542825003	chr11:49013714-49013715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183284863	chr11:49013740-49013741	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs1847644	chr11:49013741-49013742	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs141687688	chr11:49013754-49013755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574910608	chr11:49013763-49013764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs570844776	chr11:49013792-49013793	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533137117	chr11:49013814-49013815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550280915	chr11:49013827-49013828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576822082	chr11:49013835-49013836	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs570029177	chr11:49013847-49013848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs113679899	chr11:49013858-49013859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs377007180	chr11:49013859-49013860	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538876207	chr11:49015559-49015560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs7934118	chr11:49015563-49015564	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575349129	chr11:49015571-49015572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577243378	chr11:49016314-49016315	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs185142651	chr11:49016315-49016316	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs12417899	chr11:49017552-49017553	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs567937855	chr11:49017587-49017588	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs554186235	chr11:49017601-49017602	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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	17122850	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:49071400-49071600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:49098200-49098600	Enhancers	Liver	Liver
3	chr11:49110400-49112800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:49156800-49157000	Bivalent/Poised TSS	Left Ventricle	heart
5	chr11:49164200-49169200	Weak transcription	Fetal Intestine Large	intestine
6	chr11:49164600-49184200	Weak transcription	Fetal Intestine Small	intestine
7	chr11:49165600-49165800	ZNF genes & repeats	Brain Hippocampus Middle	brain
8	chr11:49165600-49167800	Weak transcription	Liver	Liver
9	chr11:49165800-49166000	Enhancers	Brain Hippocampus Middle	brain
10	chr11:49165800-49168800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr11:49166000-49184200	Weak transcription	Brain Hippocampus Middle	brain
12	chr11:49167800-49168000	Strong transcription	Liver	Liver
13	chr11:49167800-49172600	Weak transcription	Fetal Lung	lung
14	chr11:49168000-49168200	Weak transcription	Liver	Liver
15	chr11:49168200-49168400	Strong transcription	Liver	Liver
16	chr11:49168400-49169200	Weak transcription	Liver	Liver
17	chr11:49168800-49169600	Strong transcription	Duodenum Mucosa	Duodenum
18	chr11:49169200-49169600	Strong transcription	Liver	Liver
19	chr11:49169200-49169800	Strong transcription	Fetal Intestine Large	intestine
20	chr11:49169600-49174400	Weak transcription	Liver	Liver
21	chr11:49169600-49175800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr11:49169800-49170200	Weak transcription	Fetal Intestine Large	intestine
23	chr11:49170200-49171000	Strong transcription	Fetal Intestine Large	intestine
24	chr11:49171000-49172600	Weak transcription	Fetal Intestine Large	intestine
25	chr11:49171400-49197600	Weak transcription	Brain Substantia Nigra	brain
26	chr11:49171600-49190800	Weak transcription	Small Intestine	intestine
27	chr11:49172600-49173200	Strong transcription	Fetal Lung	lung
28	chr11:49172600-49173400	Strong transcription	Fetal Intestine Large	intestine
29	chr11:49173200-49184000	Weak transcription	Fetal Lung	lung
30	chr11:49173400-49177200	Weak transcription	Fetal Intestine Large	intestine
31	chr11:49174400-49176400	Strong transcription	Liver	Liver
32	chr11:49175800-49176600	Strong transcription	Duodenum Mucosa	Duodenum
33	chr11:49176200-49186800	Weak transcription	Ovary	ovary
34	chr11:49176400-49183200	Weak transcription	Liver	Liver
35	chr11:49176600-49183800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr11:49177200-49177800	Strong transcription	Fetal Intestine Large	intestine
37	chr11:49177800-49183400	Weak transcription	Fetal Intestine Large	intestine
38	chr11:49182400-49184400	Weak transcription	Fetal Stomach	stomach
39	chr11:49182800-49185200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr11:49183200-49186200	Strong transcription	Liver	Liver
41	chr11:49183400-49190000	Strong transcription	Fetal Intestine Large	intestine
42	chr11:49183800-49185600	Weak transcription	Brain Anterior Caudate	brain
43	chr11:49183800-49186800	Strong transcription	Duodenum Mucosa	Duodenum
44	chr11:49184000-49185600	Strong transcription	Fetal Lung	lung
45	chr11:49184200-49184600	Strong transcription	Fetal Intestine Small	intestine
46	chr11:49184200-49185600	Strong transcription	Brain Hippocampus Middle	brain
47	chr11:49184200-49193400	Weak transcription	Brain Cingulate Gyrus	brain
48	chr11:49184400-49185600	Strong transcription	Fetal Stomach	stomach
49	chr11:49184400-49186800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr11:49184600-49185600	ZNF genes & repeats	Fetal Intestine Small	intestine

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