Variant report

Variant	nsv972006
Chromosome Location	chr11:46449980-46451115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:46450045-46450119	K562	blood:	n/a	n/a
2	CTCF	chr11:46450208-46450455	T-47D	breast:	n/a	n/a
3	EP300	chr11:46450160-46450496	T-47D	breast:	n/a	n/a
4	FOSL2	chr11:46450175-46450475	HepG2	liver:	n/a	n/a
5	GATA2	chr11:46450062-46450737	K562	blood:	n/a	n/a
6	HEY1	chr11:46450222-46450476	HepG2	liver:	n/a	n/a
7	HEY1	chr11:46450056-46450970	K562	blood:	n/a	n/a
8	HEY1	chr11:46450576-46450975	HepG2	liver:	n/a	n/a
9	HEY1	chr11:46450582-46451013	K562	blood:	n/a	n/a
10	HEY1	chr11:46450670-46450940	HepG2	liver:	n/a	n/a
11	MYC	chr11:46450762-46450767	HepG2	liver:	n/a	n/a
12	MYC	chr11:46450681-46450943	K562	blood:	n/a	n/a
13	MYC	chr11:46450595-46450859	MCF-7	breast:	n/a	n/a
14	MYC	chr11:46450829-46450836	MCF-7	breast:	n/a	n/a
15	MYC	chr11:46450748-46450749	HUVEC	blood vessel:	n/a	n/a
16	MYC	chr11:46450546-46450972	MCF-7	breast:	n/a	n/a
17	MYC	chr11:46450686-46450738	MCF-7	breast:	n/a	n/a
18	MYC	chr11:46450777-46450854	HepG2	liver:	n/a	n/a
19	POLR2A	chr11:46450413-46451083	GM12891	blood:	n/a	n/a
20	POLR2A	chr11:46450585-46451072	U87	brain:	n/a	n/a
21	POLR2A	chr11:46450634-46451012	PANC-1	pancreas:	n/a	n/a
22	POLR2A	chr11:46450637-46450995	GM12891	blood:	n/a	n/a
23	POLR2A	chr11:46450088-46450985	GM12892	blood:	n/a	n/a
24	POLR2A	chr11:46450224-46450933	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:46450648-46450984	GM12891	blood:	n/a	n/a
26	POLR2A	chr11:46450759-46450922	A549	lung:	n/a	n/a
27	POLR2A	chr11:46450761-46451020	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr11:46450700-46451143	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr11:46450174-46450887	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr11:46450732-46450923	A549	lung:	n/a	n/a
31	POLR2A	chr11:46450652-46451119	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr11:46450435-46451196	PFSK-1	brain:	n/a	n/a
33	POLR2A	chr11:46450464-46451123	SK-N-MC	brain:	n/a	n/a
34	POLR2A	chr11:46450118-46451045	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:46450796-46450961	GM12878	blood:	n/a	n/a
36	POLR2A	chr11:46450744-46450886	A549	lung:	n/a	n/a
37	POLR2A	chr11:46450741-46450783	GM12878	blood:	n/a	n/a
38	POLR2A	chr11:46450791-46451068	ProgFib	skin:	n/a	n/a
39	POLR2A	chr11:46450203-46450443	GM12878	blood:	n/a	n/a
40	POLR2A	chr11:46450497-46451233	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:46450657-46450753	MCF-7	breast:	n/a	n/a
42	POLR2A	chr11:46450095-46450485	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:46450083-46450950	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr11:46450648-46450994	SK-N-MC	brain:	n/a	n/a
45	POLR2A	chr11:46450544-46451048	PANC-1	pancreas:	n/a	n/a
46	POLR2A	chr11:46450643-46450951	HepG2	liver:	n/a	n/a
47	POLR2A	chr11:46450649-46451072	GM12891	blood:	n/a	n/a
48	POLR2A	chr11:46450657-46450928	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:46450758-46450759	MCF-7	breast:	n/a	n/a
50	POLR2A	chr11:46450619-46451015	GM12892	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46450417-46450467	RPTEC	kidney:	n/a
2	chr11:46450417-46450467	SK-N-SH	brain:	n/a
3	chr11:46450256-46450306	AG09309	skin:	n/a
4	chr11:46450256-46450306	Caco-2	colon:	n/a
5	chr11:46450417-46450467	HL-60	blood:	n/a
6	chr11:46450417-46450467	GM12891	blood:	n/a
7	chr11:46450417-46450467	HIPEpiC	eye:	n/a
8	chr11:46450417-46450467	H1-hESC	embryonic stem cell:	embryo
9	chr11:46450417-46450467	GM12892	blood:	n/a
10	chr11:46450256-46450306	HIPEpiC	eye:	n/a
11	chr11:46450256-46450306	HRPEpiC	eye:	n/a
12	chr11:46450256-46450306	HUVEC	blood vessel:	n/a
13	chr11:46450256-46450306	NT2-D1	testis:	n/a
14	chr11:46450256-46450306	HL-60	blood:	n/a
15	chr11:46450256-46450306	NB4	blood:	n/a
16	chr11:46450256-46450306	ECC-1	luminal epithelium:	n/a
17	chr11:46450256-46450306	H1-hESC	embryonic stem cell:	embryo
18	chr11:46450256-46450306	HNPCEpiC	eye:	n/a
19	chr11:46450417-46450467	HEEpiC	esophagus:	n/a
20	chr11:46450256-46450306	PFSK-1	brain:	n/a
21	chr11:46450256-46450306	Jurkat	blood:	n/a
22	chr11:46450256-46450306	HCT-116	colon:	n/a
23	chr11:46450417-46450467	NB4	blood:	n/a
24	chr11:46450256-46450306	NH-A	brain:	n/a
25	chr11:46450417-46450467	HCF	heart:	n/a
26	chr11:46450417-46450467	GM06990	blood:	n/a
27	chr11:46450417-46450467	HRPEpiC	eye:	n/a
28	chr11:46450256-46450306	AoSMC	blood vessel:	n/a
29	chr11:46450256-46450306	ProgFib	skin:	n/a
30	chr11:46450417-46450467	Hepatocyte	liver:	n/a
31	chr11:46450256-46450306	ovcar-3	ovarian:	n/a
32	chr11:46450417-46450467	HCPEpiC	choroid plexus:	n/a
33	chr11:46450417-46450467	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:46450417-46450467	HNPCEpiC	eye:	n/a
35	chr11:46450256-46450306	LNCaP	prostate:	n/a
36	chr11:46450417-46450467	HRCEpiC	kidney:	n/a
37	chr11:46450256-46450306	U87	brain:	n/a
38	chr11:46450417-46450467	LNCaP	prostate:	n/a
39	chr11:46450417-46450467	NHDF-neo	bronchial:	n/a
40	chr11:46450417-46450467	PANC-1	pancreas:	n/a
41	chr11:46450417-46450467	ECC-1	luminal epithelium:	n/a
42	chr11:46450256-46450306	GM06990	blood:	n/a
43	chr11:46450256-46450306	Hela-S3	cervix:	n/a
44	chr11:46450417-46450467	AG10803	skin:	n/a
45	chr11:46450256-46450306	HCPEpiC	choroid plexus:	n/a
46	chr11:46450256-46450306	HEK293	kidney:	embryo
47	chr11:46450256-46450306	RPTEC	kidney:	n/a
48	chr11:46450417-46450467	HCM	heart:	n/a
49	chr11:46450417-46450467	MCF10A-Er-Src	breast:	n/a
50	chr11:46450417-46450467	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:46450716..46451228-chr6:34393228..34393955,2	HCT-116	colon:
2	chr11:46450734..46451351-chr6:34393375..34394080,2	Hela-S3	cervix:
3	chr11:46450731..46452237-chr6:34392318..34394068,7	MCF-7	breast:
4	chr11:46448160..46450143-chr11:46548223..46551067,2	MCF-7	breast:
5	chr11:46450955..46452945-chr11:46454344..46456750,3	MCF-7	breast:
6	chr11:46449211..46452238-chr6:34390894..34393967,4	K562	blood:
7	chr11:46450238..46451231-chr6:34393265..34393905,3	MCF-7	breast:
8	chr11:46449233..46452238-chr6:34392226..34393967,6	K562	blood:
9	chr11:46441415..46443647-chr11:46446607..46450426,5	K562	blood:
10	chr11:46450714..46451218-chr6:34393290..34393849,2	MCF-7	breast:
11	chr11:46450213..46450713-chr6:34392822..34393736,2	Hela-S3	cervix:
12	chr11:46449218..46452238-chr6:34392341..34394490,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000244313	TF binding region
ENSG00000244313	CpG island
ENSG00000124614	chromatin interactions
ENSG00000270800	chromatin interactions

Extended variants
information (count: 72 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568641897	chr11:46450005-46450006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs527894629	chr11:46450015-46450016	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184044137	chr11:46450016-46450017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547555887	chr11:46450055-46450056	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566232826	chr11:46450099-46450100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538306149	chr11:46450134-46450135	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528391952	chr11:46450139-46450140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs34540155	chr11:46450140-46450141	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs3179874	chr11:46450141-46450142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs201837751	chr11:46450142-46450143	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs71038902	chr11:46450152-46450153	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs3178098	chr11:46450157-46450158	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3180415	chr11:46450163-46450164	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568863082	chr11:46450167-46450168	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs537428938	chr11:46450195-46450196	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369827441	chr11:46450207-46450208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs574758112	chr11:46450229-46450230	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs188290494	chr11:46450257-46450258	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533981603	chr11:46450292-46450293	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs13264	chr11:46450293-46450294	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs11539337	chr11:46450295-46450296	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1052395	chr11:46450302-46450303	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs11556618	chr11:46450311-46450312	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1140566	chr11:46450319-46450320	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1140567	chr11:46450321-46450322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs11556617	chr11:46450324-46450325	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs17004881	chr11:46450325-46450326	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553971162	chr11:46450338-46450339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577105848	chr11:46450340-46450341	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546322406	chr11:46450349-46450350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs3210531	chr11:46450350-46450351	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562816473	chr11:46450356-46450357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576416090	chr11:46450358-46450359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541822193	chr11:46450364-46450365	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562425867	chr11:46450387-46450388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs12288189	chr11:46450388-46450389	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547594149	chr11:46450396-46450397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35234634	chr11:46450401-46450402	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533328941	chr11:46450414-46450415	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs7942614	chr11:46450433-46450434	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558423883	chr11:46450436-46450437	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537872238	chr11:46450438-46450439	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547829504	chr11:46450442-46450443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568375638	chr11:46450448-46450449	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534124404	chr11:46450527-46450528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs180702309	chr11:46450539-46450540	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs3961051	chr11:46450544-46450545	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs3975806	chr11:46450560-46450561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs577136518	chr11:46450586-46450587	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs145221216	chr11:46450638-46450639	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46417800-46463400	Weak transcription	Fetal Brain Male	brain
2	chr11:46426800-46468800	Weak transcription	Psoas Muscle	Psoas
3	chr11:46430200-46450600	Weak transcription	HUVEC	blood vessel
4	chr11:46430200-46456000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:46430600-46451600	Weak transcription	NHDF-Ad	bronchial
6	chr11:46430600-46455000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:46433600-46466400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr11:46436400-46450600	Weak transcription	Osteobl	bone
9	chr11:46436400-46454400	Weak transcription	A549	lung
10	chr11:46436600-46466400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:46437000-46452000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr11:46437200-46452600	Weak transcription	HMEC	breast
13	chr11:46437400-46455000	Weak transcription	Stomach Mucosa	stomach
14	chr11:46437600-46452600	Weak transcription	NH-A	brain
15	chr11:46437800-46450600	Weak transcription	HSMM	muscle
16	chr11:46437800-46452400	Weak transcription	Fetal Kidney	kidney
17	chr11:46438000-46461400	Strong transcription	Primary T cells from cord blood	blood
18	chr11:46438400-46451800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr11:46438400-46454400	Weak transcription	Brain Angular Gyrus	brain
20	chr11:46438400-46457200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:46438400-46459600	Strong transcription	Dnd41	blood
22	chr11:46439000-46452200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:46439000-46452800	Weak transcription	Fetal Brain Female	brain
24	chr11:46439600-46450600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:46439600-46450600	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr11:46439600-46452200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr11:46439600-46454200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:46440400-46466200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:46440600-46452600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr11:46440800-46451200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr11:46443200-46450600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:46443200-46450800	Weak transcription	Colonic Mucosa	Colon
33	chr11:46443200-46452000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:46443200-46452200	Weak transcription	Gastric	stomach
35	chr11:46443200-46452800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr11:46443200-46453000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr11:46443200-46454800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr11:46443400-46454400	Weak transcription	Brain Germinal Matrix	brain
39	chr11:46443800-46450600	Weak transcription	NHEK	skin
40	chr11:46443800-46450800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:46443800-46451000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:46443800-46451600	Weak transcription	Pancreas	Pancrea
43	chr11:46443800-46452200	Weak transcription	Brain Hippocampus Middle	brain
44	chr11:46443800-46452400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:46443800-46452400	Weak transcription	Spleen	Spleen
46	chr11:46443800-46453000	Weak transcription	Brain Cingulate Gyrus	brain
47	chr11:46443800-46454800	Weak transcription	NHLF	lung
48	chr11:46444000-46450400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:46444000-46450600	Weak transcription	Hela-S3	cervix
50	chr11:46444000-46450800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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