Variant report

Variant	nsv591350
Chromosome Location	chr3:118719480-118823141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:754)
CpG islands
(count:918)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	ARID3A	chr3:118734227-118734231	HepG2	liver:	n/a	n/a
3	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
4	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
5	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
7	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
8	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
9	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
10	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
11	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
13	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
14	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
15	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
16	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
17	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
18	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
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	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
23	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
24	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:118817520-118817670	HCM	heart:	n/a	chr3:118817652-118817670
26	CTCF	chr3:118753740-118753890	A549	lung:	n/a	n/a
27	CTCF	chr3:118753671-118753970	GM10266	blood:	n/a	n/a
28	CTCF	chr3:118753447-118754025	GM12892	blood:	n/a	n/a
29	CTCF	chr3:118804020-118804170	GM12873	blood:	n/a	n/a
30	CTCF	chr3:118817600-118817750	HEK293	kidney:	n/a	chr3:118817652-118817670
31	CTCF	chr3:118753540-118753690	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:118817536-118817759	Kidney_OC	kidney:	n/a	chr3:118817652-118817670
33	CTCF	chr3:118817440-118817911	A549	lung:	n/a	chr3:118817652-118817670
34	CTCF	chr3:118753740-118753890	GM12871	blood:	n/a	n/a
35	CTCF	chr3:118817463-118817853	ECC-1	luminal epithelium:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118817329-118818055	SK-N-SH	brain:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118817580-118817730	HCPEpiC	choroid plexus:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118753565-118754007	GM12891	blood:	n/a	n/a
39	CTCF	chr3:118816907-118818485	A549	lung:	n/a	chr3:118817652-118817670
40	CTCF	chr3:118804040-118804190	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:118817540-118817690	BE2_C	brain:	n/a	chr3:118817652-118817670
42	CTCF	chr3:118753700-118753850	Caco-2	colon:	n/a	n/a
43	CTCF	chr3:118753380-118753530	GM12864	blood:	n/a	n/a
44	CTCF	chr3:118753491-118754113	K562	blood:	n/a	n/a
45	CTCF	chr3:118817560-118817710	GM12878	blood:	n/a	chr3:118817652-118817670
46	CTCF	chr3:118817443-118817882	GM12878	blood:	n/a	chr3:118817652-118817670
47	CTCF	chr3:118753729-118754017	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:118754000-118754150	GM12867	blood:	n/a	n/a
49	CTCF	chr3:118817580-118817730	NHEK	skin:	n/a	chr3:118817652-118817670
50	CTCF	chr3:118753720-118753870	AG04450	lung:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118734756-118734806	HRPEpiC	eye:	n/a
2	chr3:118753871-118753921	HepG2	liver:	n/a
3	chr3:118753871-118753921	GM12892	blood:	n/a
4	chr3:118734756-118734806	HRPEpiC	eye:	n/a
5	chr3:118753871-118753921	HepG2	liver:	n/a
6	chr3:118753871-118753921	GM12892	blood:	n/a
7	chr3:118754097-118754147	ovcar-3	ovarian:	n/a
8	chr3:118753738-118753788	HMEC	breast:	n/a
9	chr3:118750463-118750513	AG04449	skin:	fetal
10	chr3:118750463-118750513	H1-hESC	embryonic stem cell:	embryo
11	chr3:118754097-118754147	AG09309	skin:	n/a
12	chr3:118753660-118753710	CMK	blood:	n/a
13	chr3:118753660-118753710	ProgFib	skin:	n/a
14	chr3:118792317-118792367	HEK293	kidney:	embryo
15	chr3:118734756-118734806	HEEpiC	esophagus:	n/a
16	chr3:118750463-118750513	HAEpiC	amniotic membrane:	n/a
17	chr3:118753738-118753788	SKMC	muscle:	n/a
18	chr3:118753093-118753143	H1-hESC	embryonic stem cell:	embryo
19	chr3:118754376-118754426	HepG2	liver:	n/a
20	chr3:118753714-118753764	GM12878	blood:	n/a
21	chr3:118753005-118753055	IMR90	lung:	fetal
22	chr3:118753005-118753055	GM19239	blood:	n/a
23	chr3:118753738-118753788	PANC-1	pancreas:	n/a
24	chr3:118753093-118753143	HCF	heart:	n/a
25	chr3:118754097-118754147	GM19239	blood:	n/a
26	chr3:118753738-118753788	U87	brain:	n/a
27	chr3:118792317-118792367	LNCaP	prostate:	n/a
28	chr3:118754376-118754426	NHDF-neo	bronchial:	n/a
29	chr3:118734756-118734806	HCF	heart:	n/a
30	chr3:118757898-118757948	HNPCEpiC	eye:	n/a
31	chr3:118757898-118757948	HMEC	breast:	n/a
32	chr3:118753610-118753660	BJ	skin:	n/a
33	chr3:118734756-118734806	Hela-S3	cervix:	n/a
34	chr3:118753705-118753755	HUVEC	blood vessel:	n/a
35	chr3:118753705-118753755	GM12878	blood:	n/a
36	chr3:118754097-118754147	RPTEC	kidney:	n/a
37	chr3:118753660-118753710	HRPEpiC	eye:	n/a
38	chr3:118734756-118734806	PFSK-1	brain:	n/a
39	chr3:118753005-118753055	NB4	blood:	n/a
40	chr3:118753005-118753055	AG09319	gingival:	n/a
41	chr3:118754376-118754426	AoSMC	blood vessel:	n/a
42	chr3:118753871-118753921	NHDF-neo	bronchial:	n/a
43	chr3:118757898-118757948	AG09309	skin:	n/a
44	chr3:118757898-118757948	U87	brain:	n/a
45	chr3:118753005-118753055	GM12891	blood:	n/a
46	chr3:118757898-118757948	NH-A	brain:	n/a
47	chr3:118753707-118753757	LNCaP	prostate:	n/a
48	chr3:118753714-118753764	Hela-S3	cervix:	n/a
49	chr3:118753871-118753921	Caco-2	colon:	n/a
50	chr3:118753871-118753921	HNPCEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
2	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
3	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
4	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
5	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
6	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
7	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
8	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
9	chr3:118601491..118603517-chr3:118818904..118820959,2	MCF-7	breast:
10	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
11	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
12	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
13	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
14	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
15	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
16	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
17	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
18	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:

No data

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

Extended variants
information (count: 2116 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2116 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4687835	chr3:118719480-118719481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532434819	chr3:118719483-118719484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2215812	chr3:118719485-118719486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544572567	chr3:118719505-118719506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562887225	chr3:118719524-118719525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190900204	chr3:118719573-118719574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201888716	chr3:118719580-118719581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548662715	chr3:118719584-118719585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375549456	chr3:118719648-118719649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566676717	chr3:118719653-118719654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199923025	chr3:118719692-118719693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552204077	chr3:118719722-118719723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570711934	chr3:118719739-118719740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537475208	chr3:118719784-118719785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556122501	chr3:118719806-118719807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567858285	chr3:118719810-118719811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535178311	chr3:118719812-118719813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553421615	chr3:118719843-118719844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573114836	chr3:118719852-118719853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112188046	chr3:118719853-118719854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146028575	chr3:118719876-118719877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577462349	chr3:118719880-118719881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138725797	chr3:118719908-118719909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149325993	chr3:118719931-118719932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182943805	chr3:118719943-118719944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542364734	chr3:118719956-118719957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560538636	chr3:118719986-118719987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527528272	chr3:118719990-118719991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552329902	chr3:118719993-118719994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564271824	chr3:118719996-118719997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7641626	chr3:118720016-118720017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529200175	chr3:118720020-118720021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376585708	chr3:118720034-118720035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549760386	chr3:118720062-118720063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548959764	chr3:118720102-118720103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73185827	chr3:118720107-118720108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567737238	chr3:118720179-118720180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535047538	chr3:118720184-118720185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569255662	chr3:118720198-118720199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185787439	chr3:118720219-118720220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547122605	chr3:118720241-118720242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370246147	chr3:118720243-118720244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190990230	chr3:118720247-118720248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534173712	chr3:118720280-118720281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11924178	chr3:118720293-118720294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577325295	chr3:118720295-118720296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147175391	chr3:118720310-118720311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374810064	chr3:118720314-118720315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368550323	chr3:118720315-118720316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556867470	chr3:118720332-118720333	Weak transcription	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:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118713000-118727000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:118713800-118719800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:118715400-118731800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:118716600-118720000	Weak transcription	Brain Anterior Caudate	brain
5	chr3:118716800-118729000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:118717200-118719800	Weak transcription	Brain Substantia Nigra	brain
7	chr3:118719800-118720200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:118719800-118720200	Enhancers	Brain Substantia Nigra	brain
9	chr3:118720000-118720200	Enhancers	Brain Anterior Caudate	brain
10	chr3:118720200-118726600	Weak transcription	Brain Substantia Nigra	brain
11	chr3:118720200-118727000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:118725000-118727400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:118725200-118737600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:118726200-118727800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr3:118726400-118726600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:118726400-118726800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr3:118726400-118726800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr3:118726400-118728600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:118726600-118727400	Enhancers	Brain Substantia Nigra	brain
20	chr3:118727000-118729600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
21	chr3:118727000-118729600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:118727200-118731600	Weak transcription	Psoas Muscle	Psoas
23	chr3:118727400-118727800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:118727400-118730800	Weak transcription	Brain Substantia Nigra	brain
25	chr3:118727400-118731600	Weak transcription	Ovary	ovary
26	chr3:118727800-118728200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:118727800-118734400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:118728600-118729000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:118729000-118729600	Enhancers	Brain Anterior Caudate	brain
30	chr3:118729000-118729600	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr3:118729600-118730400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:118729600-118730800	Weak transcription	Brain Anterior Caudate	brain
33	chr3:118729600-118730800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr3:118729600-118732800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr3:118730000-118742000	Enhancers	Brain Angular Gyrus	brain
36	chr3:118730400-118730600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr3:118730600-118731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:118730800-118731000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr3:118730800-118731400	Active TSS	Stomach Smooth Muscle	stomach
40	chr3:118730800-118732000	Enhancers	Brain Hippocampus Middle	brain
41	chr3:118730800-118736400	Enhancers	Fetal Brain Male	brain
42	chr3:118730800-118738600	Enhancers	Brain Anterior Caudate	brain
43	chr3:118730800-118741800	Enhancers	Brain Substantia Nigra	brain
44	chr3:118731000-118731400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr3:118731200-118731400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:118731400-118732200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:118731400-118734200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr3:118731600-118732000	Enhancers	Psoas Muscle	Psoas

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