Variant report

Variant	nsv980228
Chromosome Location	chr4:87834452-87845024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87843493-87843868	HepG2	liver:	n/a	n/a
2	BACH1	chr4:87844411-87844418	K562	blood:	n/a	n/a
3	BCLAF1	chr4:87843486-87843924	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:87839862-87840034	K562	blood:	n/a	n/a
5	BHLHE40	chr4:87843564-87843866	GM12878	blood:	n/a	n/a
6	CCNT2	chr4:87837536-87837788	K562	blood:	n/a	n/a
7	CCNT2	chr4:87843723-87843953	K562	blood:	n/a	n/a
8	CEBPB	chr4:87842871-87843129	H1-hESC	embryonic stem cell:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
9	CEBPB	chr4:87839973-87840306	HepG2	liver:	n/a	chr4:87840139-87840150
10	CEBPB	chr4:87838995-87839295	HepG2	liver:	n/a	chr4:87839138-87839149
11	CEBPB	chr4:87843544-87843864	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:87840014-87840210	HepG2	liver:	n/a	chr4:87840139-87840150
13	CEBPB	chr4:87840012-87840253	HepG2	liver:	n/a	chr4:87840139-87840150
14	CEBPB	chr4:87838953-87839278	K562	blood:	n/a	chr4:87839138-87839149
15	CEBPB	chr4:87842781-87843114	IMR90	lung:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
16	CEBPB	chr4:87842784-87843058	HepG2	liver:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
17	CEBPB	chr4:87839959-87840315	IMR90	lung:	n/a	chr4:87840139-87840150
18	CEBPB	chr4:87839066-87839293	IMR90	lung:	n/a	chr4:87839138-87839149
19	CEBPB	chr4:87843591-87843930	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:87842854-87843119	MCF-7	breast:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
21	CEBPB	chr4:87841000-87841328	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:87838951-87839260	Hela-S3	cervix:	n/a	chr4:87839138-87839149
23	CEBPB	chr4:87842782-87843079	A549	lung:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
24	CEBPB	chr4:87842782-87843143	K562	blood:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
25	CEBPB	chr4:87838877-87839325	K562	blood:	n/a	chr4:87839138-87839149
26	CEBPB	chr4:87843495-87843895	K562	blood:	n/a	n/a
27	CEBPB	chr4:87843500-87843984	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:87842741-87843178	Hela-S3	cervix:	n/a	chr4:87842966-87842977 chr4:87842898-87842909
29	CEBPB	chr4:87837574-87837852	K562	blood:	n/a	n/a
30	CEBPD	chr4:87837426-87837993	K562	blood:	n/a	n/a
31	CEBPD	chr4:87837408-87837907	K562	blood:	n/a	n/a
32	CHD2	chr4:87843539-87843925	GM12878	blood:	n/a	n/a
33	CTCF	chr4:87843660-87843810	HRE	kidney:	n/a	n/a
34	CTCF	chr4:87843640-87843790	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr4:87842620-87842770	AG10803	skin:	n/a	n/a
36	CTCF	chr4:87843640-87843790	AG10803	skin:	n/a	n/a
37	CTCF	chr4:87843640-87843790	AG04449	skin:	n/a	n/a
38	CTCF	chr4:87843591-87843905	GM19239	blood:	n/a	n/a
39	CTCF	chr4:87843535-87843846	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr4:87843600-87843750	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:87843660-87843810	GM12868	blood:	n/a	n/a
42	CTCF	chr4:87843660-87843810	HCM	heart:	n/a	n/a
43	CTCF	chr4:87843562-87843939	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:87843640-87843790	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:87843540-87843910	HepG2	liver:	n/a	n/a
46	CTCF	chr4:87843660-87843810	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:87843640-87843790	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:87843620-87843770	GM12875	blood:	n/a	n/a
49	CTCF	chr4:87843629-87843965	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:87843980-87844130	AG10803	skin:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:87843821..87845327-chr4:88013319..88016028,2	MCF-7	breast:
2	chr4:87840562..87842094-chr4:87856459..87858099,2	MCF-7	breast:
3	chr4:87843608..87844207-chr4:88156694..88157622,2	K562	blood:
4	chr4:87842227..87846817-chr4:87925967..87929277,6	MCF-7	breast:
5	chr4:87843646..87844235-chr4:88071692..88072390,2	K562	blood:
6	chr4:87843404..87844119-chr4:87882783..87883663,2	MCF-7	breast:
7	chr4:87831738..87834823-chr4:87927716..87932272,4	K562	blood:
8	chr4:87832559..87834802-chr4:87929759..87932272,2	K562	blood:
9	chr4:87842585..87845353-chr4:87979775..87981630,2	K562	blood:
10	chr4:87831113..87833915-chr4:87837544..87840445,2	K562	blood:
11	chr4:87836003..87837844-chr4:88123291..88126235,2	K562	blood:
12	chr4:87843288..87844189-chr4:88013665..88015393,4	K562	blood:
13	chr4:87843422..87844230-chr4:88014418..88015268,4	MCF-7	breast:
14	chr4:87833323..87835057-chr4:87926520..87929216,2	K562	blood:
15	chr4:87834231..87835806-chr4:87836450..87839189,2	K562	blood:
16	chr4:87842485..87845250-chr4:87926450..87930883,7	K562	blood:
17	chr4:87841127..87845186-chr4:87926504..87931446,8	K562	blood:
18	chr4:87843259..87843829-chr4:88156202..88157194,2	MCF-7	breast:
19	chr4:87843214..87843994-chr4:88014244..88015104,4	MCF-7	breast:
20	chr4:87843366..87844046-chr4:87927469..87928269,2	MCF-7	breast:
21	chr4:87842431..87844252-chr4:87926551..87928246,2	MCF-7	breast:
22	chr4:87834231..87835806-chr4:87836450..87839189,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A6-1	chr4:87835853-87835970	NONHSAT097288
2	lnc-SLC10A6-2	chr4:87843242-87844887	NONHSAT097289
3	lnc-SLC10A6-1	chr4:87835118-87835541	NONHSAT097288
4	lnc-SLC10A6-1	chr4:87834419-87834986	NONHSAT097288

No data

Variant related genes	Relation type
ENSG00000251411	TF binding region
ENSG00000172493	chromatin interactions
ENSG00000163633	chromatin interactions

Extended variants
information (count: 424 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375444769	chr4:87834496-87834497	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs531356734	chr4:87834545-87834546	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs532232093	chr4:87834573-87834574	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs549956924	chr4:87834584-87834585	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs17751557	chr4:87834607-87834608	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532466962	chr4:87834618-87834619	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs551470104	chr4:87834627-87834628	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs376489745	chr4:87834628-87834629	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs138933632	chr4:87834649-87834650	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs369494803	chr4:87834661-87834662	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs555853134	chr4:87834668-87834669	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568839588	chr4:87834684-87834685	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs538022189	chr4:87834687-87834688	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs373262481	chr4:87834703-87834704	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs2594276	chr4:87834762-87834763	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs578169741	chr4:87834779-87834780	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs76549645	chr4:87834801-87834802	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs545716204	chr4:87834837-87834838	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs35622795	chr4:87834878-87834879	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs553476014	chr4:87834897-87834898	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs371737172	chr4:87834930-87834931	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs34247749	chr4:87834979-87834980	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs4693153	chr4:87835005-87835006	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542218478	chr4:87835006-87835007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560607846	chr4:87835008-87835009	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531320186	chr4:87835025-87835026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543231414	chr4:87835036-87835037	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565123353	chr4:87835050-87835051	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532296798	chr4:87835051-87835052	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547716337	chr4:87835066-87835067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565986100	chr4:87835078-87835079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527647481	chr4:87835090-87835091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549416377	chr4:87835114-87835115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567736351	chr4:87835162-87835163	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs538362549	chr4:87835182-87835183	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs556463419	chr4:87835183-87835184	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs571847960	chr4:87835186-87835187	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs538957409	chr4:87835217-87835218	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs553997836	chr4:87835219-87835220	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs553895609	chr4:87835267-87835268	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs72876047	chr4:87835305-87835306	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs542181458	chr4:87835318-87835319	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs554173675	chr4:87835330-87835331	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs13149781	chr4:87835412-87835413	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs13149977	chr4:87835413-87835414	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs567850673	chr4:87835446-87835447	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs189541288	chr4:87835449-87835450	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs11550145	chr4:87835461-87835462	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs536491262	chr4:87835475-87835476	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs13125924	chr4:87835477-87835478	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87825600-87838800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:87825600-87846000	Weak transcription	Gastric	stomach
3	chr4:87825600-87849400	Weak transcription	Lung	lung
4	chr4:87825600-87849400	Weak transcription	Spleen	Spleen
5	chr4:87825800-87839400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:87825800-87843600	Weak transcription	Brain Anterior Caudate	brain
7	chr4:87825800-87854800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr4:87825800-87854800	Weak transcription	Right Ventricle	heart
9	chr4:87825800-87855200	Weak transcription	Fetal Stomach	stomach
10	chr4:87826000-87852400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr4:87826200-87841000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:87826200-87843000	Weak transcription	Liver	Liver
13	chr4:87826200-87843400	Weak transcription	Brain Substantia Nigra	brain
14	chr4:87829200-87839800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:87829800-87855000	Weak transcription	Aorta	Aorta
16	chr4:87830200-87849600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr4:87830200-87855200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr4:87830400-87847600	Weak transcription	Thymus	Thymus
19	chr4:87830400-87847800	Weak transcription	Psoas Muscle	Psoas
20	chr4:87830400-87849400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr4:87830400-87854600	Weak transcription	Brain Hippocampus Middle	brain
22	chr4:87830600-87839400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:87830600-87839400	Weak transcription	Adipose Nuclei	Adipose
24	chr4:87830600-87843000	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr4:87830600-87843400	Weak transcription	Colon Smooth Muscle	Colon
26	chr4:87830600-87843400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:87830600-87845600	Weak transcription	Left Ventricle	heart
28	chr4:87831000-87855000	Weak transcription	Fetal Lung	lung
29	chr4:87831400-87854400	Weak transcription	Fetal Heart	heart
30	chr4:87831400-87854800	Weak transcription	Right Atrium	heart
31	chr4:87831800-87840200	Weak transcription	Primary B cells from cord blood	blood
32	chr4:87832200-87854800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr4:87832800-87840200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr4:87833000-87834600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:87833000-87837000	Weak transcription	Placenta	Placenta
36	chr4:87833000-87838600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr4:87833000-87839600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:87833800-87838800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr4:87834200-87835400	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr4:87834400-87835200	Strong transcription	Fetal Intestine Small	intestine
41	chr4:87834400-87835200	Strong transcription	Pancreas	Pancrea
42	chr4:87834600-87834800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:87834800-87838200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:87835200-87836000	Weak transcription	Fetal Intestine Small	intestine
45	chr4:87835200-87849000	Weak transcription	Pancreas	Pancrea
46	chr4:87835400-87839800	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr4:87836000-87836400	Strong transcription	Fetal Intestine Small	intestine
48	chr4:87836200-87836400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:87836400-87837800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:87836400-87839200	Weak transcription	Fetal Intestine Small	intestine

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