Variant report

Variant	nsv1013684
Chromosome Location	chr3:118734931-118817646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:857)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
2	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
3	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
4	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
6	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
7	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
8	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
9	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
10	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
13	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
14	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
15	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
16	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
17	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
19	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
20	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
21	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
23	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr3:118753720-118753870	GM12873	blood:	n/a	n/a
25	CTCF	chr3:118753720-118753870	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr3:118753760-118753910	HVMF	connective:	n/a	n/a
27	CTCF	chr3:118753500-118753650	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr3:118753460-118753610	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr3:118804080-118804230	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:118817600-118817750	BE2_C	brain:	n/a	chr3:118817652-118817670
31	CTCF	chr3:118753514-118753971	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:118803991-118804179	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:118817600-118817750	GM06990	blood:	n/a	chr3:118817652-118817670
34	CTCF	chr3:118753494-118753981	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:118753740-118753890	BE2_C	brain:	n/a	n/a
36	CTCF	chr3:118804060-118804210	GM12872	blood:	n/a	n/a
37	CTCF	chr3:118753740-118753890	GM06990	blood:	n/a	n/a
38	CTCF	chr3:118753720-118753870	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:118753520-118753670	A549	lung:	n/a	n/a
40	CTCF	chr3:118753520-118753670	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr3:118817580-118817730	HCPEpiC	choroid plexus:	n/a	chr3:118817652-118817670
42	CTCF	chr3:118813748-118813757	ProgFib	skin:	n/a	n/a
43	CTCF	chr3:118753700-118753850	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr3:118753520-118753670	GM06990	blood:	n/a	n/a
45	CTCF	chr3:118753700-118753850	AG09319	gingival:	n/a	n/a
46	CTCF	chr3:118804114-118804120	HepG2	liver:	n/a	n/a
47	CTCF	chr3:118804040-118804190	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:118817560-118817710	GM12867	blood:	n/a	chr3:118817652-118817670
49	CTCF	chr3:118817620-118817770	HRPEpiC	eye:	n/a	chr3:118817652-118817670
50	CTCF	chr3:118817600-118817750	AG10803	skin:	n/a	chr3:118817652-118817670

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118754376-118754426	MCF10A-Er-Src	breast:	n/a
2	chr3:118750463-118750513	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:118753093-118753143	Jurkat	blood:	n/a
4	chr3:118754376-118754426	MCF10A-Er-Src	breast:	n/a
5	chr3:118750463-118750513	HPAEpiC	pulmonary alveolar:	n/a
6	chr3:118753093-118753143	Jurkat	blood:	n/a
7	chr3:118753005-118753055	HEK293	kidney:	embryo
8	chr3:118750463-118750513	SKMC	muscle:	n/a
9	chr3:118753738-118753788	Hela-S3	cervix:	n/a
10	chr3:118753738-118753788	PANC-1	pancreas:	n/a
11	chr3:118757898-118757948	NB4	blood:	n/a
12	chr3:118753871-118753921	AG09319	gingival:	n/a
13	chr3:118753714-118753764	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:118753707-118753757	HRCEpiC	kidney:	n/a
15	chr3:118754097-118754147	HRCEpiC	kidney:	n/a
16	chr3:118792317-118792367	AG04450	lung:	fetal
17	chr3:118754376-118754426	SK-N-SH	brain:	n/a
18	chr3:118753005-118753055	HAEpiC	amniotic membrane:	n/a
19	chr3:118754097-118754147	NHDF-neo	bronchial:	n/a
20	chr3:118754097-118754147	SKMC	muscle:	n/a
21	chr3:118753871-118753921	AoSMC	blood vessel:	n/a
22	chr3:118754376-118754426	HAEpiC	amniotic membrane:	n/a
23	chr3:118757898-118757948	H1-hESC	embryonic stem cell:	embryo
24	chr3:118753714-118753764	PrEC	prostate:	n/a
25	chr3:118753705-118753755	HRPEpiC	eye:	n/a
26	chr3:118753707-118753757	AG09319	gingival:	n/a
27	chr3:118753660-118753710	A549	lung:	n/a
28	chr3:118753660-118753710	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:118753871-118753921	MCF10A-Er-Src	breast:	n/a
30	chr3:118753005-118753055	CMK	blood:	n/a
31	chr3:118750463-118750513	PFSK-1	brain:	n/a
32	chr3:118750463-118750513	HIPEpiC	eye:	n/a
33	chr3:118753610-118753660	SK-N-SH	brain:	n/a
34	chr3:118754097-118754147	PANC-1	pancreas:	n/a
35	chr3:118753005-118753055	SK-N-MC	brain:	n/a
36	chr3:118757898-118757948	U87	brain:	n/a
37	chr3:118792317-118792367	HAEpiC	amniotic membrane:	n/a
38	chr3:118792317-118792367	HMEC	breast:	n/a
39	chr3:118750463-118750513	Caco-2	colon:	n/a
40	chr3:118753660-118753710	AoSMC	blood vessel:	n/a
41	chr3:118753871-118753921	GM12892	blood:	n/a
42	chr3:118753714-118753764	HAEpiC	amniotic membrane:	n/a
43	chr3:118753714-118753764	Jurkat	blood:	n/a
44	chr3:118753093-118753143	MCF-7	breast:	n/a
45	chr3:118753610-118753660	AG04450	lung:	fetal
46	chr3:118757898-118757948	GM12892	blood:	n/a
47	chr3:118753610-118753660	AG09319	gingival:	n/a
48	chr3:118792317-118792367	ECC-1	luminal epithelium:	n/a
49	chr3:118754376-118754426	HMEC	breast:	n/a
50	chr3:118753660-118753710	NT2-D1	testis:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
2	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
3	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
4	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
5	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
6	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
7	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
8	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
9	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
10	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
11	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
12	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
13	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
14	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
15	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
16	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
17	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000144847	chromatin interactions
ENSG00000232429	chromatin interactions

Extended variants
information (count: 1465 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185688945	chr3:118734947-118734948	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs12053925	chr3:118735022-118735023	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs141685433	chr3:118735026-118735027	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs150499880	chr3:118735027-118735028	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs386665087	chr3:118735031-118735032	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544740874	chr3:118735032-118735033	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs114215046	chr3:118735056-118735057	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs76964840	chr3:118735076-118735077	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs139473176	chr3:118735117-118735118	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560444645	chr3:118735130-118735131	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs41497149	chr3:118735159-118735160	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs371473258	chr3:118735177-118735178	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs563752343	chr3:118735202-118735203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531177923	chr3:118735222-118735223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549873444	chr3:118735226-118735227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142220311	chr3:118735235-118735236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373029931	chr3:118735253-118735254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530367773	chr3:118735268-118735269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548502936	chr3:118735326-118735327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567017093	chr3:118735367-118735368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534513918	chr3:118735378-118735379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552876694	chr3:118735407-118735408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs10934472	chr3:118735409-118735410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs71325355	chr3:118735416-118735417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556658113	chr3:118735423-118735424	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs574832937	chr3:118735519-118735520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs574775207	chr3:118735552-118735553	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs9860826	chr3:118735567-118735568	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146402934	chr3:118735568-118735569	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs545713036	chr3:118735581-118735582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs139683126	chr3:118735618-118735619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs144450624	chr3:118735711-118735712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs543049440	chr3:118735745-118735746	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs190486548	chr3:118735769-118735770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs180944394	chr3:118735776-118735777	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs1435664	chr3:118735820-118735821	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560690441	chr3:118735845-118735846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6438482	chr3:118735849-118735850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1435665	chr3:118735853-118735854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145351577	chr3:118735881-118735882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs60190891	chr3:118735886-118735887	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs373714095	chr3:118735887-118735888	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs1435666	chr3:118735916-118735917	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549911332	chr3:118735939-118735940	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568401883	chr3:118735951-118735952	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535590671	chr3:118735956-118735957	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs554207254	chr3:118735979-118735980	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78535437	chr3:118736002-118736003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184882703	chr3:118736005-118736006	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs148732725	chr3:118736098-118736099	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118725200-118737600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:118730000-118742000	Enhancers	Brain Angular Gyrus	brain
3	chr3:118730800-118736400	Enhancers	Fetal Brain Male	brain
4	chr3:118730800-118738600	Enhancers	Brain Anterior Caudate	brain
5	chr3:118730800-118741800	Enhancers	Brain Substantia Nigra	brain
6	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr3:118731800-118736200	Enhancers	Brain Cingulate Gyrus	brain
9	chr3:118732000-118737600	Weak transcription	Psoas Muscle	Psoas
10	chr3:118732600-118735200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:118733000-118740000	Enhancers	Brain Hippocampus Middle	brain
12	chr3:118733200-118735200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr3:118734200-118735000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:118734400-118735000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr3:118734600-118735000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr3:118734600-118735000	Enhancers	Ovary	ovary
17	chr3:118734600-118735200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:118734600-118735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:118734600-118736000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr3:118734800-118735000	Enhancers	Brain Germinal Matrix	brain
21	chr3:118734800-118735200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:118734800-118735200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:118734800-118735200	Enhancers	Pancreas	Pancrea
24	chr3:118734800-118736000	Enhancers	Fetal Brain Female	brain
25	chr3:118735000-118735200	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr3:118735000-118736200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:118735000-118737400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:118735000-118737600	Weak transcription	Ovary	ovary
29	chr3:118735200-118735400	Enhancers	Brain Germinal Matrix	brain
30	chr3:118735200-118735600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr3:118735200-118738000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr3:118735200-118738200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr3:118735200-118738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:118735200-118739000	Weak transcription	Pancreas	Pancrea
35	chr3:118735400-118735800	Flanking Active TSS	Brain Germinal Matrix	brain
36	chr3:118735600-118735800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr3:118735800-118738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr3:118735800-118739600	Enhancers	Brain Germinal Matrix	brain
39	chr3:118736000-118737000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr3:118736000-118737600	Weak transcription	Fetal Brain Female	brain
41	chr3:118736200-118736600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr3:118736200-118738200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:118736400-118736800	Weak transcription	Fetal Brain Male	brain
44	chr3:118736600-118744400	Enhancers	Brain Cingulate Gyrus	brain
45	chr3:118736800-118740000	Enhancers	Fetal Brain Male	brain
46	chr3:118737000-118738200	Enhancers	Stomach Smooth Muscle	stomach
47	chr3:118737000-118741200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr3:118737200-118738400	Enhancers	A549	lung
49	chr3:118737400-118738200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr3:118737400-118739400	Enhancers	Fetal Heart	heart

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