Variant report

Variant	nsv591391
Chromosome Location	chr3:119403145-119442572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:586)
CpG islands
(count:733)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:119435954-119436321	HepG2	liver:	n/a	n/a
2	ATF2	chr3:119419260-119419790	GM12878	blood:	n/a	n/a
3	ATF2	chr3:119415949-119416762	GM12878	blood:	n/a	n/a
4	ATF2	chr3:119419112-119419861	GM12878	blood:	n/a	n/a
5	ATF2	chr3:119416135-119416799	GM12878	blood:	n/a	n/a
6	BACH1	chr3:119421256-119421985	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr3:119416187-119416633	GM12878	blood:	n/a	n/a
8	BATF	chr3:119419396-119419828	GM12878	blood:	n/a	chr3:119419597-119419608
9	BATF	chr3:119416221-119416736	GM12878	blood:	n/a	n/a
10	BATF	chr3:119419338-119419885	GM12878	blood:	n/a	chr3:119419597-119419608
11	BCL11A	chr3:119416282-119416662	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:119419397-119419785	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:119416224-119416686	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:119419296-119419881	GM12878	blood:	n/a	n/a
15	BCL3	chr3:119419304-119419795	GM12878	blood:	n/a	n/a
16	BCL3	chr3:119416216-119416654	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:119416117-119416732	GM12878	blood:	n/a	chr3:119416198-119416207
18	BCLAF1	chr3:119419226-119419743	GM12878	blood:	n/a	n/a
19	BCLAF1	chr3:119416131-119416727	GM12878	blood:	n/a	chr3:119416198-119416207
20	BHLHE40	chr3:119416183-119416597	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:119421891-119421929	GM12878	blood:	n/a	n/a
22	BRCA1	chr3:119421750-119421757	GM12878	blood:	n/a	n/a
23	BRCA1	chr3:119421512-119422038	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr3:119414331-119414620	K562	blood:	n/a	n/a
25	CBX3	chr3:119414383-119414656	K562	blood:	n/a	n/a
26	CEBPB	chr3:119408860-119409068	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:119418818-119419942	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:119414351-119414670	K562	blood:	n/a	n/a
29	CEBPB	chr3:119408747-119409002	K562	blood:	n/a	n/a
30	CEBPB	chr3:119414351-119414804	A549	lung:	n/a	n/a
31	CEBPB	chr3:119434784-119435021	HepG2	liver:	n/a	chr3:119434897-119434908 chr3:119434981-119434992
32	CEBPB	chr3:119419950-119420073	K562	blood:	n/a	n/a
33	CEBPB	chr3:119408865-119409057	A549	lung:	n/a	n/a
34	CEBPZ	chr3:119404012-119404021	HepG2	liver:	n/a	n/a
35	CHD1	chr3:119422148-119422153	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr3:119421447-119422044	GM12878	blood:	n/a	chr3:119421549-119421559 chr3:119421542-119421552
37	CHD2	chr3:119421455-119422185	H1-hESC	embryonic stem cell:	n/a	chr3:119421549-119421559 chr3:119421542-119421552
38	CHD2	chr3:119419385-119419743	GM12878	blood:	n/a	n/a
39	CHD2	chr3:119416259-119416603	GM12878	blood:	n/a	n/a
40	CTCF	chr3:119409015-119409195	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr3:119409016-119409150	Lung_OC	lung:	n/a	n/a
42	CTCF	chr3:119409040-119409190	GM12875	blood:	n/a	n/a
43	CTCF	chr3:119408960-119409230	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr3:119430508-119430578	Hela-S3	cervix:	n/a	chr3:119430535-119430556 chr3:119430541-119430557
45	CTCF	chr3:119408980-119409130	GM12870	blood:	n/a	n/a
46	CTCF	chr3:119409000-119409150	RPTEC	kidney:	n/a	n/a
47	CTCF	chr3:119409099-119409171	GM19239	blood:	n/a	n/a
48	CTCF	chr3:119409040-119409190	HL-60	blood:	n/a	n/a
49	CTCF	chr3:119408740-119408890	GM12867	blood:	n/a	n/a
50	CTCF	chr3:119405520-119405554	GM19240	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119421614-119421664	HRPEpiC	eye:	n/a
2	chr3:119421614-119421664	HRPEpiC	eye:	n/a
3	chr3:119419493-119419543	GM12892	blood:	n/a
4	chr3:119422283-119422333	ECC-1	luminal epithelium:	n/a
5	chr3:119421614-119421664	LNCaP	prostate:	n/a
6	chr3:119420208-119420258	HRE	kidney:	n/a
7	chr3:119421868-119421918	PANC-1	pancreas:	n/a
8	chr3:119420208-119420258	SK-N-SH	brain:	n/a
9	chr3:119421868-119421918	ovcar-3	ovarian:	n/a
10	chr3:119421604-119421654	RPTEC	kidney:	n/a
11	chr3:119421667-119421717	SK-N-MC	brain:	n/a
12	chr3:119421553-119421603	HUVEC	blood vessel:	n/a
13	chr3:119420208-119420258	SKMC	muscle:	n/a
14	chr3:119421604-119421654	HEEpiC	esophagus:	n/a
15	chr3:119421939-119421989	HAEpiC	amniotic membrane:	n/a
16	chr3:119421553-119421603	Hepatocyte	liver:	n/a
17	chr3:119422359-119422409	Jurkat	blood:	n/a
18	chr3:119421939-119421989	MCF10A-Er-Src	breast:	n/a
19	chr3:119421614-119421664	GM12878	blood:	n/a
20	chr3:119421868-119421918	HRCEpiC	kidney:	n/a
21	chr3:119420208-119420258	SK-N-MC	brain:	n/a
22	chr3:119425176-119425226	BE2_C	brain:	n/a
23	chr3:119421614-119421664	HRCEpiC	kidney:	n/a
24	chr3:119421667-119421717	GM12892	blood:	n/a
25	chr3:119420208-119420258	HUVEC	blood vessel:	n/a
26	chr3:119420208-119420258	IMR90	lung:	fetal
27	chr3:119421614-119421664	HCPEpiC	choroid plexus:	n/a
28	chr3:119419493-119419543	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:119421868-119421918	HUVEC	blood vessel:	n/a
30	chr3:119421667-119421717	PFSK-1	brain:	n/a
31	chr3:119421868-119421918	AG04450	lung:	fetal
32	chr3:119421939-119421989	SK-N-SH_RA	brain:	n/a
33	chr3:119422161-119422211	NB4	blood:	n/a
34	chr3:119425176-119425226	GM19239	blood:	n/a
35	chr3:119419493-119419543	ovcar-3	ovarian:	n/a
36	chr3:119422283-119422333	HL-60	blood:	n/a
37	chr3:119421667-119421717	AG04450	lung:	fetal
38	chr3:119421553-119421603	HCT-116	colon:	n/a
39	chr3:119421667-119421717	SKMC	muscle:	n/a
40	chr3:119421868-119421918	HNPCEpiC	eye:	n/a
41	chr3:119421868-119421918	SK-N-SH	brain:	n/a
42	chr3:119421939-119421989	PrEC	prostate:	n/a
43	chr3:119421553-119421603	NB4	blood:	n/a
44	chr3:119422161-119422211	SK-N-SH_RA	brain:	n/a
45	chr3:119421614-119421664	MCF-7	breast:	n/a
46	chr3:119421553-119421603	AG09319	gingival:	n/a
47	chr3:119419493-119419543	H1-hESC	embryonic stem cell:	embryo
48	chr3:119421553-119421603	GM19239	blood:	n/a
49	chr3:119421614-119421664	K562	blood:	n/a
50	chr3:119421667-119421717	H1-hESC	embryonic stem cell:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:119408612..119410162-chr3:119814493..119816849,2	K562	blood:
2	chr3:119393569..119396281-chr3:119421855..119424087,2	MCF-7	breast:
3	chr3:119422857..119424567-chr7:75925278..75927867,2	MCF-7	breast:
4	chr3:119440802..119443470-chr3:119448061..119449825,2	K562	blood:
5	chr3:119394872..119397577-chr3:119400469..119404472,3	MCF-7	breast:
6	chr3:119397978..119400630-chr3:119401218..119403216,2	MCF-7	breast:
7	chr3:118876250..118878600-chr3:119400821..119403241,2	MCF-7	breast:
8	chr3:119413495..119415805-chr3:119419920..119422060,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAATS1	TF binding region
MAATS1	CpG island
ENSG00000183833	chromatin interactions
ENSG00000138495	chromatin interactions

Extended variants
information (count: 1476 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1476 , 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	rs6809361	chr3:119403145-119403146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs145713873	chr3:119403157-119403158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560894886	chr3:119403224-119403225	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs34644899	chr3:119403263-119403264	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528209182	chr3:119403309-119403310	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6785906	chr3:119403350-119403351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546340079	chr3:119403361-119403362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368401347	chr3:119403396-119403397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545757193	chr3:119403416-119403417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs66802265	chr3:119403428-119403429	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs551695974	chr3:119403436-119403437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188288993	chr3:119403451-119403452	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537272212	chr3:119403525-119403526	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144201180	chr3:119403547-119403548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561276495	chr3:119403609-119403610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374399517	chr3:119403619-119403620	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs180702582	chr3:119403629-119403630	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186395831	chr3:119403643-119403644	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553144079	chr3:119403649-119403650	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs578001942	chr3:119403760-119403761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545406410	chr3:119403783-119403784	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189742038	chr3:119403805-119403806	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575634841	chr3:119403825-119403826	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs542599655	chr3:119403826-119403827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542911082	chr3:119403837-119403838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561148055	chr3:119403855-119403856	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181204916	chr3:119403870-119403871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs530217274	chr3:119403886-119403887	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189798824	chr3:119403923-119403924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532010928	chr3:119403968-119403969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9917775	chr3:119403995-119403996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2688645	chr3:119404008-119404009	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs531124814	chr3:119404015-119404016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549370046	chr3:119404026-119404027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9822052	chr3:119404058-119404059	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534898776	chr3:119404124-119404125	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146764890	chr3:119404181-119404182	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571749027	chr3:119404209-119404210	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34775086	chr3:119404233-119404234	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs75696216	chr3:119404240-119404241	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371527807	chr3:119404276-119404277	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs76422775	chr3:119404286-119404287	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187123553	chr3:119404292-119404293	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527409272	chr3:119404307-119404308	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573032278	chr3:119404335-119404336	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190472755	chr3:119404358-119404359	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6789375	chr3:119404359-119404360	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs576548951	chr3:119404367-119404368	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111342791	chr3:119404375-119404376	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562153963	chr3:119404436-119404437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
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
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119404200-119404400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:119404400-119405400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:119405400-119406000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:119406000-119421400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:119415800-119416000	Enhancers	GM12878-XiMat	blood
6	chr3:119416000-119416600	Flanking Active TSS	GM12878-XiMat	blood
7	chr3:119416600-119418400	Enhancers	GM12878-XiMat	blood
8	chr3:119418200-119418400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr3:119418400-119421200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:119418400-119422200	ZNF genes & repeats	GM12878-XiMat	blood
11	chr3:119418800-119421400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr3:119419000-119419200	Enhancers	Placenta	Placenta
13	chr3:119419000-119419400	Enhancers	Stomach Mucosa	stomach
14	chr3:119419000-119420800	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr3:119419000-119421200	Enhancers	Adipose Nuclei	Adipose
16	chr3:119419000-119421200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr3:119419000-119421400	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:119419000-119421400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr3:119419000-119421400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr3:119419000-119421400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr3:119419000-119421400	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr3:119419200-119419400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr3:119419200-119419600	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr3:119419200-119419600	Enhancers	A549	lung
25	chr3:119419200-119420200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr3:119419200-119420600	Enhancers	Primary T cells fromperipheralblood	blood
27	chr3:119419200-119420600	Enhancers	HUVEC	blood vessel
28	chr3:119419200-119420800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:119419200-119420800	Enhancers	Left Ventricle	heart
30	chr3:119419200-119420800	Enhancers	Small Intestine	intestine
31	chr3:119419200-119421200	Enhancers	Duodenum Mucosa	Duodenum
32	chr3:119419200-119421400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr3:119419200-119421400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr3:119419400-119419600	Enhancers	Primary B cells from cord blood	blood
35	chr3:119419400-119419600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:119419400-119420000	Enhancers	K562	blood
37	chr3:119419400-119420400	Weak transcription	Placenta	Placenta
38	chr3:119419400-119421200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr3:119419400-119421400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr3:119419400-119421400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr3:119419400-119421400	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr3:119419400-119421400	Weak transcription	Stomach Mucosa	stomach
43	chr3:119419600-119419800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr3:119419600-119420000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr3:119419600-119420400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:119419600-119421200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:119419600-119421200	Weak transcription	Right Ventricle	heart
48	chr3:119419600-119421200	Weak transcription	A549	lung
49	chr3:119419600-119421400	Enhancers	Liver	Liver
50	chr3:119419800-119420000	Enhancers	Primary B cells from cord blood	blood

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