Variant report

Variant	nsv1004498
Chromosome Location	chr3:118735159-118818041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:726)
CpG islands
(count:854)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:726 , 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	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
9	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
10	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
13	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
14	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
15	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
16	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
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	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
20	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
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	chr3:118817570-118817740	H1-hESC	embryonic stem cell:	n/a	chr3:118817652-118817670
25	CTCF	chr3:118753680-118753830	HRE	kidney:	n/a	n/a
26	CTCF	chr3:118753720-118753870	GM12865	blood:	n/a	n/a
27	CTCF	chr3:118753760-118753910	GM12867	blood:	n/a	n/a
28	CTCF	chr3:118753780-118753930	GM12864	blood:	n/a	n/a
29	CTCF	chr3:118817560-118817710	HUVEC	blood vessel:	n/a	chr3:118817652-118817670
30	CTCF	chr3:118754260-118754410	HRE	kidney:	n/a	n/a
31	CTCF	chr3:118753517-118754027	GM19239	blood:	n/a	n/a
32	CTCF	chr3:118817486-118817815	SK-N-SH_RA	brain:	n/a	chr3:118817652-118817670
33	CTCF	chr3:118817600-118817750	Caco-2	colon:	n/a	chr3:118817652-118817670
34	CTCF	chr3:118753720-118753870	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr3:118753780-118753930	GM12866	blood:	n/a	n/a
36	CTCF	chr3:118753729-118754017	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:118817600-118817750	GM06990	blood:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118817600-118817750	GM12866	blood:	n/a	chr3:118817652-118817670
39	CTCF	chr3:118753760-118753910	NB4	blood:	n/a	n/a
40	CTCF	chr3:118753719-118753957	GM20000	blood:	n/a	n/a
41	CTCF	chr3:118754000-118754150	GM06990	blood:	n/a	n/a
42	CTCF	chr3:118817580-118817730	HRPEpiC	eye:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118753691-118753967	A549	lung:	n/a	n/a
44	CTCF	chr3:118753760-118753910	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr3:118753580-118753730	HFF	foreskin:	n/a	n/a
46	CTCF	chr3:118804080-118804230	A549	lung:	n/a	n/a
47	CTCF	chr3:118804092-118804100	GM12878	blood:	n/a	n/a
48	CTCF	chr3:118817580-118817730	WI-38	lung:	n/a	chr3:118817652-118817670
49	CTCF	chr3:118753521-118753966	HepG2	liver:	n/a	n/a
50	CTCF	chr3:118817500-118817650	WI-38	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753738-118753788	HMEC	breast:	n/a
2	chr3:118754376-118754426	SK-N-SH_RA	brain:	n/a
3	chr3:118753738-118753788	NB4	blood:	n/a
4	chr3:118753660-118753710	K562	blood:	n/a
5	chr3:118757898-118757948	K562	blood:	n/a
6	chr3:118757898-118757948	SK-N-SH_RA	brain:	n/a
7	chr3:118750463-118750513	GM12878	blood:	n/a
8	chr3:118753871-118753921	SK-N-MC	brain:	n/a
9	chr3:118753705-118753755	H1-hESC	embryonic stem cell:	embryo
10	chr3:118754376-118754426	ProgFib	skin:	n/a
11	chr3:118753705-118753755	HRCEpiC	kidney:	n/a
12	chr3:118753705-118753755	GM12892	blood:	n/a
13	chr3:118753610-118753660	GM12891	blood:	n/a
14	chr3:118753714-118753764	ovcar-3	ovarian:	n/a
15	chr3:118792317-118792367	Hela-S3	cervix:	n/a
16	chr3:118757898-118757948	SK-N-SH	brain:	n/a
17	chr3:118753871-118753921	GM12891	blood:	n/a
18	chr3:118754376-118754426	PFSK-1	brain:	n/a
19	chr3:118753707-118753757	HRCEpiC	kidney:	n/a
20	chr3:118754097-118754147	HEK293	kidney:	embryo
21	chr3:118753093-118753143	T-47D	breast:	n/a
22	chr3:118757898-118757948	BE2_C	brain:	n/a
23	chr3:118754097-118754147	H1-hESC	embryonic stem cell:	embryo
24	chr3:118754097-118754147	Hela-S3	cervix:	n/a
25	chr3:118754097-118754147	LNCaP	prostate:	n/a
26	chr3:118753093-118753143	AG10803	skin:	n/a
27	chr3:118753610-118753660	RPTEC	kidney:	n/a
28	chr3:118753871-118753921	HCT-116	colon:	n/a
29	chr3:118753714-118753764	U87	brain:	n/a
30	chr3:118750463-118750513	AG04449	skin:	fetal
31	chr3:118754097-118754147	AG04449	skin:	fetal
32	chr3:118753738-118753788	Jurkat	blood:	n/a
33	chr3:118753707-118753757	NH-A	brain:	n/a
34	chr3:118753871-118753921	NH-A	brain:	n/a
35	chr3:118753093-118753143	MCF10A-Er-Src	breast:	n/a
36	chr3:118757898-118757948	SKMC	muscle:	n/a
37	chr3:118753093-118753143	PrEC	prostate:	n/a
38	chr3:118792317-118792367	AG04449	skin:	fetal
39	chr3:118754376-118754426	HL-60	blood:	n/a
40	chr3:118753738-118753788	AoSMC	blood vessel:	n/a
41	chr3:118753707-118753757	A549	lung:	n/a
42	chr3:118753093-118753143	HRCEpiC	kidney:	n/a
43	chr3:118753005-118753055	HCT-116	colon:	n/a
44	chr3:118792317-118792367	HEK293	kidney:	embryo
45	chr3:118753660-118753710	SKMC	muscle:	n/a
46	chr3:118750463-118750513	HCT-116	colon:	n/a
47	chr3:118753738-118753788	A549	lung:	n/a
48	chr3:118754376-118754426	LNCaP	prostate:	n/a
49	chr3:118792317-118792367	GM12878	blood:	n/a
50	chr3:118753738-118753788	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
2	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
3	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
4	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
5	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
6	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
7	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
8	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
9	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
10	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
11	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
12	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
13	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
14	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
15	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
16	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
17	chr3:118781130..118783547-chr3:118786161..118788492,2	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: 1467 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1467 , 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	rs41497149	chr3:118735159-118735160	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371473258	chr3:118735177-118735178	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs563752343	chr3:118735202-118735203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531177923	chr3:118735222-118735223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549873444	chr3:118735226-118735227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142220311	chr3:118735235-118735236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373029931	chr3:118735253-118735254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530367773	chr3:118735268-118735269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548502936	chr3:118735326-118735327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567017093	chr3:118735367-118735368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534513918	chr3:118735378-118735379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552876694	chr3:118735407-118735408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs10934472	chr3:118735409-118735410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs71325355	chr3:118735416-118735417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556658113	chr3:118735423-118735424	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs574832937	chr3:118735519-118735520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574775207	chr3:118735552-118735553	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs9860826	chr3:118735567-118735568	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs146402934	chr3:118735568-118735569	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545713036	chr3:118735581-118735582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs139683126	chr3:118735618-118735619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs144450624	chr3:118735711-118735712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs543049440	chr3:118735745-118735746	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190486548	chr3:118735769-118735770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs180944394	chr3:118735776-118735777	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs1435664	chr3:118735820-118735821	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560690441	chr3:118735845-118735846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6438482	chr3:118735849-118735850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs1435665	chr3:118735853-118735854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145351577	chr3:118735881-118735882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs60190891	chr3:118735886-118735887	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs373714095	chr3:118735887-118735888	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs1435666	chr3:118735916-118735917	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549911332	chr3:118735939-118735940	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568401883	chr3:118735951-118735952	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535590671	chr3:118735956-118735957	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs554207254	chr3:118735979-118735980	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs78535437	chr3:118736002-118736003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs184882703	chr3:118736005-118736006	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs148732725	chr3:118736098-118736099	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529142797	chr3:118736169-118736170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115966595	chr3:118736184-118736185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561547725	chr3:118736231-118736232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372769085	chr3:118736281-118736282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540796933	chr3:118736282-118736283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559991379	chr3:118736283-118736284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559476888	chr3:118736299-118736300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527931228	chr3:118736327-118736328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115853606	chr3:118736361-118736362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75795507	chr3:118736381-118736382	Weak transcription Enhancers	n/a	n/a	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:533 , 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	chr3:118734600-118735200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr3:118734600-118735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr3:118734600-118736000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:118734800-118735200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:118734800-118735200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:118734800-118735200	Enhancers	Pancreas	Pancrea
19	chr3:118734800-118736000	Enhancers	Fetal Brain Female	brain
20	chr3:118735000-118735200	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr3:118735000-118736200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:118735000-118737400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:118735000-118737600	Weak transcription	Ovary	ovary
24	chr3:118735200-118735400	Enhancers	Brain Germinal Matrix	brain
25	chr3:118735200-118735600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr3:118735200-118738000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr3:118735200-118738200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr3:118735200-118738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:118735200-118739000	Weak transcription	Pancreas	Pancrea
30	chr3:118735400-118735800	Flanking Active TSS	Brain Germinal Matrix	brain
31	chr3:118735600-118735800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr3:118735800-118738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr3:118735800-118739600	Enhancers	Brain Germinal Matrix	brain
34	chr3:118736000-118737000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr3:118736000-118737600	Weak transcription	Fetal Brain Female	brain
36	chr3:118736200-118736600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr3:118736200-118738200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:118736400-118736800	Weak transcription	Fetal Brain Male	brain
39	chr3:118736600-118744400	Enhancers	Brain Cingulate Gyrus	brain
40	chr3:118736800-118740000	Enhancers	Fetal Brain Male	brain
41	chr3:118737000-118738200	Enhancers	Stomach Smooth Muscle	stomach
42	chr3:118737000-118741200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr3:118737200-118738400	Enhancers	A549	lung
44	chr3:118737400-118738200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr3:118737400-118739400	Enhancers	Fetal Heart	heart
46	chr3:118737400-118739600	Enhancers	Colon Smooth Muscle	Colon
47	chr3:118737400-118740000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:118737600-118737800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr3:118737600-118737800	Enhancers	Psoas Muscle	Psoas
50	chr3:118737600-118738400	Enhancers	Skeletal Muscle Male	skeletal muscle

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