Variant report

Variant	nsv967070
Chromosome Location	chr3:138355155-138372373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138356593-138356595	HepG2	liver:	n/a	n/a
2	BACH1	chr3:138363584-138363681	K562	blood:	n/a	n/a
3	CBX3	chr3:138360272-138360625	K562	blood:	n/a	n/a
4	CBX3	chr3:138361105-138362027	K562	blood:	n/a	n/a
5	CBX3	chr3:138365353-138365708	K562	blood:	n/a	n/a
6	CBX3	chr3:138359525-138359800	K562	blood:	n/a	n/a
7	CBX3	chr3:138367766-138368604	K562	blood:	n/a	n/a
8	CBX3	chr3:138361122-138362091	K562	blood:	n/a	n/a
9	CEBPB	chr3:138362555-138362646	K562	blood:	n/a	n/a
10	CHD2	chr3:138363372-138363654	K562	blood:	n/a	n/a
11	CHD2	chr3:138368864-138369102	K562	blood:	n/a	n/a
12	CHD2	chr3:138368084-138368163	HepG2	liver:	n/a	n/a
13	CTCF	chr3:138357500-138357589	Lung_OC	lung:	n/a	n/a
14	E2F6	chr3:138365361-138365766	H1-hESC	embryonic stem cell:	n/a	n/a
15	E2F6	chr3:138361415-138361642	K562	blood:	n/a	n/a
16	E2F6	chr3:138364603-138364702	K562	blood:	n/a	n/a
17	E2F6	chr3:138362782-138362913	K562	blood:	n/a	n/a
18	E2F6	chr3:138367934-138368226	K562	blood:	n/a	n/a
19	E2F6	chr3:138368254-138368457	K562	blood:	n/a	n/a
20	E2F6	chr3:138361321-138362030	H1-hESC	embryonic stem cell:	n/a	n/a
21	E2F6	chr3:138364718-138365355	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr3:138363358-138363769	H1-hESC	embryonic stem cell:	n/a	n/a
23	FOS	chr3:138359454-138359759	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr3:138359425-138359755	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr3:138359426-138359786	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr3:138359447-138359712	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr3:138356543-138356734	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:138356693-138356723	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr3:138362964-138363608	HepG2	liver:	n/a	n/a
30	FOSL2	chr3:138367838-138369015	HepG2	liver:	n/a	n/a
31	GATA3	chr3:138359431-138359751	T-47D	breast:	n/a	n/a
32	GTF2F1	chr3:138367853-138368183	H1-hESC	embryonic stem cell:	n/a	n/a
33	GTF2F1	chr3:138364813-138365688	H1-hESC	embryonic stem cell:	n/a	n/a
34	GTF2F1	chr3:138361043-138361354	H1-hESC	embryonic stem cell:	n/a	n/a
35	GTF2F1	chr3:138361209-138361557	K562	blood:	n/a	n/a
36	GTF2F1	chr3:138364846-138365494	K562	blood:	n/a	n/a
37	GTF2F1	chr3:138364256-138364344	H1-hESC	embryonic stem cell:	n/a	n/a
38	GTF2F1	chr3:138363230-138363659	H1-hESC	embryonic stem cell:	n/a	n/a
39	GTF2F1	chr3:138370087-138370222	H1-hESC	embryonic stem cell:	n/a	n/a
40	GTF2F1	chr3:138368036-138368157	K562	blood:	n/a	n/a
41	IRF1	chr3:138364283-138364298	K562	blood:	n/a	n/a
42	JUN	chr3:138364195-138364357	K562	blood:	n/a	n/a
43	JUND	chr3:138359426-138359631	K562	blood:	n/a	n/a
44	JUND	chr3:138369695-138369894	HepG2	liver:	n/a	chr3:138369760-138369771
45	KAP1	chr3:138364339-138364632	K562	blood:	n/a	n/a
46	KAP1	chr3:138365257-138365734	K562	blood:	n/a	n/a
47	KAP1	chr3:138361608-138362054	K562	blood:	n/a	n/a
48	MAX	chr3:138367960-138368205	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAX	chr3:138364885-138365262	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAX	chr3:138360319-138360582	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138363566-138363616	LNCaP	prostate:	n/a
2	chr3:138363566-138363616	HepG2	liver:	n/a
3	chr3:138363566-138363616	NH-A	brain:	n/a
4	chr3:138363566-138363616	HEEpiC	esophagus:	n/a
5	chr3:138363566-138363616	HNPCEpiC	eye:	n/a
6	chr3:138363566-138363616	SK-N-MC	brain:	n/a
7	chr3:138363566-138363616	PANC-1	pancreas:	n/a
8	chr3:138363566-138363616	Caco-2	colon:	n/a
9	chr3:138363566-138363616	ECC-1	luminal epithelium:	n/a
10	chr3:138363566-138363616	AG10803	skin:	n/a
11	chr3:138363566-138363616	AG09319	gingival:	n/a
12	chr3:138363566-138363616	A549	lung:	n/a
13	chr3:138363566-138363616	MCF-7	breast:	n/a
14	chr3:138363566-138363616	MCF10A-Er-Src	breast:	n/a
15	chr3:138363566-138363616	GM12878	blood:	n/a
16	chr3:138363566-138363616	PFSK-1	brain:	n/a
17	chr3:138363566-138363616	HRPEpiC	eye:	n/a
18	chr3:138363566-138363616	Hela-S3	cervix:	n/a
19	chr3:138363566-138363616	K562	blood:	n/a
20	chr3:138363566-138363616	GM12891	blood:	n/a
21	chr3:138363566-138363616	BE2_C	brain:	n/a
22	chr3:138363566-138363616	SK-N-SH	brain:	n/a
23	chr3:138363566-138363616	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:138363566-138363616	NT2-D1	testis:	n/a
25	chr3:138363566-138363616	AG09309	skin:	n/a
26	chr3:138363566-138363616	HCPEpiC	choroid plexus:	n/a
27	chr3:138363566-138363616	AG04449	skin:	fetal
28	chr3:138363566-138363616	IMR90	lung:	fetal
29	chr3:138363566-138363616	HAEpiC	amniotic membrane:	n/a
30	chr3:138363566-138363616	ovcar-3	ovarian:	n/a
31	chr3:138363566-138363616	GM19239	blood:	n/a
32	chr3:138363566-138363616	HEK293	kidney:	embryo
33	chr3:138363566-138363616	BJ	skin:	n/a
34	chr3:138363566-138363616	HCF	heart:	n/a
35	chr3:138363566-138363616	NHDF-neo	bronchial:	n/a
36	chr3:138363566-138363616	HIPEpiC	eye:	n/a
37	chr3:138363566-138363616	CMK	blood:	n/a
38	chr3:138363566-138363616	HL-60	blood:	n/a
39	chr3:138363566-138363616	Jurkat	blood:	n/a
40	chr3:138363566-138363616	SKMC	muscle:	n/a
41	chr3:138363566-138363616	AG04450	lung:	fetal
42	chr3:138363566-138363616	Hepatocyte	liver:	n/a
43	chr3:138363566-138363616	HUVEC	blood vessel:	n/a
44	chr3:138363566-138363616	GM12892	blood:	n/a
45	chr3:138363566-138363616	ProgFib	skin:	n/a
46	chr3:138363566-138363616	U87	brain:	n/a
47	chr3:138363566-138363616	PrEC	prostate:	n/a
48	chr3:138363566-138363616	HRE	kidney:	n/a
49	chr3:138363566-138363616	HRCEpiC	kidney:	n/a
50	chr3:138363566-138363616	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:138336729..138341143-chr3:138355200..138358307,3	K562	blood:
2	chr3:138352958..138355851-chr3:138357963..138360391,2	K562	blood:
3	chr3:138355271..138356796-chr3:138371743..138374136,2	K562	blood:
4	chr3:138366382..138369111-chr3:138372165..138373999,2	K562	blood:
5	chr3:138355271..138356796-chr3:138371743..138374136,2	K562	blood:
6	chr3:138327416..138329320-chr3:138370308..138373534,3	MCF-7	breast:
7	chr3:138366382..138369561-chr3:138372165..138374975,3	K562	blood:
8	chr3:138366382..138369561-chr3:138372165..138374975,3	K562	blood:
9	chr3:138369214..138371379-chr3:138655274..138656934,2	K562	blood:
10	chr3:138327553..138329730-chr3:138368846..138371731,2	K562	blood:
11	chr3:138328883..138330750-chr3:138369541..138371730,2	MCF-7	breast:
12	chr3:138352958..138355851-chr3:138357963..138360391,2	K562	blood:
13	chr3:138366382..138369111-chr3:138372165..138373999,2	K562	blood:
14	chr3:138351784..138353339-chr3:138356450..138359152,2	K562	blood:
15	chr3:138354512..138356684-chr3:138362796..138364936,2	K562	blood:
16	chr3:138347442..138349226-chr3:138355499..138357103,2	K562	blood:
17	chr3:138363143..138366102-chr3:138366258..138369219,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAIM-3	chr3:138363668-138365757	NONHSAT092338

No data

Variant related genes	Relation type
ENSG00000174715	TF binding region
ENSG00000174715	CpG island
ENSG00000174715	chromatin interactions
ENSG00000158234	chromatin interactions

Extended variants
information (count: 685 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34426677	chr3:138355183-138355184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527769538	chr3:138355202-138355203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs111796013	chr3:138355286-138355287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567485344	chr3:138355307-138355308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs192221057	chr3:138355332-138355333	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561131448	chr3:138355349-138355350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529789918	chr3:138355374-138355375	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184796795	chr3:138355390-138355391	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569588102	chr3:138355430-138355431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187916562	chr3:138355432-138355433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201366124	chr3:138355447-138355448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs57851017	chr3:138355448-138355449	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536538955	chr3:138355487-138355488	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141229609	chr3:138355554-138355555	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs565583415	chr3:138355557-138355558	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs361057	chr3:138355606-138355607	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs554322409	chr3:138355656-138355657	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs645240	chr3:138355693-138355694	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs645237	chr3:138355695-138355696	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs666888	chr3:138355702-138355703	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs377535626	chr3:138355724-138355725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536809160	chr3:138355745-138355746	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111765624	chr3:138355781-138355782	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538423911	chr3:138355799-138355800	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533334713	chr3:138355800-138355801	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558246427	chr3:138355824-138355825	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs571780198	chr3:138355837-138355838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs187243	chr3:138355848-138355849	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs139490103	chr3:138355850-138355851	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs143390459	chr3:138355863-138355864	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545750390	chr3:138355885-138355886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558902441	chr3:138355982-138355983	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201971074	chr3:138355996-138355997	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572392646	chr3:138356030-138356031	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541417115	chr3:138356056-138356057	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191276938	chr3:138356064-138356065	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147540618	chr3:138356065-138356066	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369786090	chr3:138356109-138356110	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs34338454	chr3:138356111-138356112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs202142632	chr3:138356174-138356175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs369311620	chr3:138356200-138356201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543193411	chr3:138356231-138356232	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184442856	chr3:138356247-138356248	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115230354	chr3:138356288-138356289	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554325617	chr3:138356300-138356301	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs373219917	chr3:138356341-138356342	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs552236389	chr3:138356362-138356363	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565967858	chr3:138356393-138356394	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116683862	chr3:138356416-138356417	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2607796	chr3:138356417-138356418	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:53)

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	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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138328600-138358000	Weak transcription	Psoas Muscle	Psoas
2	chr3:138328800-138358000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:138335400-138368000	Weak transcription	Right Ventricle	heart
4	chr3:138337000-138360400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:138340400-138393800	Weak transcription	Fetal Brain Male	brain
6	chr3:138341200-138355800	Weak transcription	Dnd41	blood
7	chr3:138341800-138355200	Weak transcription	Primary B cells from cord blood	blood
8	chr3:138342400-138362200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:138342600-138356400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:138345000-138356600	Weak transcription	HSMMtube	muscle
11	chr3:138345000-138367800	Weak transcription	HSMM	muscle
12	chr3:138345200-138357600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:138345200-138357600	Weak transcription	Spleen	Spleen
14	chr3:138345400-138355600	Weak transcription	NH-A	brain
15	chr3:138345400-138361600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:138345400-138368000	Weak transcription	NHLF	lung
17	chr3:138345600-138356600	Weak transcription	Brain Substantia Nigra	brain
18	chr3:138345600-138367400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr3:138345800-138368000	Weak transcription	HMEC	breast
20	chr3:138346600-138356200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr3:138346600-138357800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr3:138348600-138355600	Weak transcription	Fetal Intestine Large	intestine
23	chr3:138348800-138357800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr3:138348800-138368000	Weak transcription	Hela-S3	cervix
25	chr3:138349000-138358200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:138349000-138367400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr3:138349000-138368000	Weak transcription	Pancreas	Pancrea
28	chr3:138349200-138355600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr3:138350400-138355200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr3:138350800-138355200	Weak transcription	Fetal Thymus	thymus
31	chr3:138350800-138362800	Weak transcription	Thymus	Thymus
32	chr3:138350800-138367800	Weak transcription	Osteobl	bone
33	chr3:138351000-138357400	Weak transcription	Aorta	Aorta
34	chr3:138351400-138356600	Weak transcription	Left Ventricle	heart
35	chr3:138351400-138367800	Weak transcription	Ovary	ovary
36	chr3:138352000-138361000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:138352800-138357000	Weak transcription	Lung	lung
38	chr3:138353000-138357400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr3:138353000-138361600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:138353000-138367800	Weak transcription	Fetal Kidney	kidney
41	chr3:138353000-138368200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr3:138353200-138357000	Weak transcription	Adipose Nuclei	Adipose
43	chr3:138353200-138357600	Weak transcription	Fetal Muscle Leg	muscle
44	chr3:138353400-138355800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:138353400-138356800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:138354600-138355400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:138354600-138357200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:138355400-138358400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr3:138356800-138358000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:138357600-138358000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links