Variant report

Variant	nsv878109
Chromosome Location	chr3:191178925-191227296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 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	chr3:191191432-191192143	K562	blood:	n/a	n/a
2	ARID3A	chr3:191209628-191209646	K562	blood:	n/a	n/a
3	ATF3	chr3:191194161-191194511	K562	blood:	n/a	n/a
4	BACH1	chr3:191191387-191191876	K562	blood:	n/a	n/a
5	BHLHE40	chr3:191191581-191191624	K562	blood:	n/a	n/a
6	BHLHE40	chr3:191217493-191217797	K562	blood:	n/a	n/a
7	CBX3	chr3:191217458-191217812	K562	blood:	n/a	n/a
8	CBX3	chr3:191201840-191202240	K562	blood:	n/a	n/a
9	CCNT2	chr3:191217369-191217837	K562	blood:	n/a	n/a
10	CEBPB	chr3:191203369-191203725	K562	blood:	n/a	n/a
11	CEBPB	chr3:191188359-191188642	K562	blood:	n/a	n/a
12	CEBPB	chr3:191202309-191202710	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:191218718-191219075	H1-hESC	embryonic stem cell:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
14	CEBPB	chr3:191218711-191219079	K562	blood:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
15	CEBPB	chr3:191191421-191191601	K562	blood:	n/a	n/a
16	CEBPB	chr3:191191338-191191926	K562	blood:	n/a	n/a
17	CEBPB	chr3:191207415-191207435	K562	blood:	n/a	n/a
18	CEBPB	chr3:191218714-191219055	HepG2	liver:	n/a	chr3:191218865-191218876 chr3:191218896-191218907
19	CEBPB	chr3:191191384-191191970	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:191221034-191221300	HepG2	liver:	n/a	chr3:191221178-191221189 chr3:191221177-191221190
21	CEBPB	chr3:191191372-191191877	K562	blood:	n/a	n/a
22	CTCF	chr3:191220480-191220630	BE2_C	brain:	n/a	chr3:191220559-191220580
23	CTCF	chr3:191220460-191220610	AG04449	skin:	n/a	chr3:191220559-191220580
24	CTCF	chr3:191220480-191220630	SK-N-SH_RA	brain:	n/a	chr3:191220559-191220580
25	CTCF	chr3:191220480-191220630	HEK293	kidney:	n/a	chr3:191220559-191220580
26	CTCF	chr3:191220448-191220691	MCF-7	breast:	n/a	chr3:191220559-191220580
27	CTCF	chr3:191220486-191220645	Kidney_OC	kidney:	n/a	chr3:191220559-191220580
28	CTCF	chr3:191220480-191220630	HRE	kidney:	n/a	chr3:191220559-191220580
29	CTCF	chr3:191220340-191220490	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr3:191220520-191220670	GM12873	blood:	n/a	chr3:191220559-191220580
31	CTCF	chr3:191220695-191220700	LNCaP	prostate:	n/a	n/a
32	CTCF	chr3:191220500-191220650	Hela-S3	cervix:	n/a	chr3:191220559-191220580
33	CTCF	chr3:191220471-191220671	T-47D	breast:	n/a	chr3:191220559-191220580
34	CTCF	chr3:191220543-191220584	MCF-7	breast:	n/a	chr3:191220559-191220580
35	CTCF	chr3:191220465-191220668	Hela-S3	cervix:	n/a	chr3:191220559-191220580
36	CTCF	chr3:191217631-191217634	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:191220500-191220650	HepG2	liver:	n/a	chr3:191220559-191220580
38	CTCF	chr3:191220460-191220610	GM06990	blood:	n/a	chr3:191220559-191220580
39	CTCF	chr3:191220480-191220630	HPAF	blood vessel:	n/a	chr3:191220559-191220580
40	CTCF	chr3:191193955-191194034	Fibrobl	skin:	n/a	n/a
41	CTCF	chr3:191220440-191220590	HCT-116	colon:	n/a	chr3:191220559-191220580
42	CTCF	chr3:191220480-191220630	HCPEpiC	choroid plexus:	n/a	chr3:191220559-191220580
43	CTCF	chr3:191220480-191220630	GM12865	blood:	n/a	chr3:191220559-191220580
44	CTCF	chr3:191220500-191220650	GM12872	blood:	n/a	chr3:191220559-191220580
45	CTCF	chr3:191220455-191220693	LNCaP	prostate:	n/a	chr3:191220559-191220580
46	CTCF	chr3:191220507-191220606	GM13977	blood:	n/a	chr3:191220559-191220580
47	CTCF	chr3:191220499-191220631	Medullo	brain:	n/a	chr3:191220559-191220580
48	CTCF	chr3:191220540-191220690	HFF	foreskin:	n/a	chr3:191220559-191220580
49	CTCF	chr3:191220440-191220590	WERI-Rb-1	eye:	n/a	chr3:191220559-191220580
50	CTCF	chr3:191220480-191220630	HMF	breast:	n/a	chr3:191220559-191220580

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191179074-191179124	NB4	blood:	n/a
2	chr3:191178924-191178974	SAEC	small airway:	n/a
3	chr3:191178924-191178974	HCM	heart:	n/a
4	chr3:191179074-191179124	HepG2	liver:	n/a
5	chr3:191178924-191178974	GM06990	blood:	n/a
6	chr3:191179074-191179124	AG04450	lung:	fetal
7	chr3:191179074-191179124	A549	lung:	n/a
8	chr3:191179074-191179124	HCM	heart:	n/a
9	chr3:191178924-191178974	LNCaP	prostate:	n/a
10	chr3:191179074-191179124	GM06990	blood:	n/a
11	chr3:191178924-191178974	HepG2	liver:	n/a
12	chr3:191179074-191179124	BE2_C	brain:	n/a
13	chr3:191179074-191179124	SK-N-MC	brain:	n/a
14	chr3:191178924-191178974	Hela-S3	cervix:	n/a
15	chr3:191178924-191178974	HEEpiC	esophagus:	n/a
16	chr3:191179074-191179124	PrEC	prostate:	n/a
17	chr3:191179074-191179124	ovcar-3	ovarian:	n/a
18	chr3:191178924-191178974	RPTEC	kidney:	n/a
19	chr3:191179074-191179124	AG04449	skin:	fetal
20	chr3:191178924-191178974	AG04449	skin:	fetal
21	chr3:191179074-191179124	NHBE	bronchial:	n/a
22	chr3:191179074-191179124	GM12892	blood:	n/a
23	chr3:191178924-191178974	NHBE	bronchial:	n/a
24	chr3:191178924-191178974	HCF	heart:	n/a
25	chr3:191178924-191178974	IMR90	lung:	fetal
26	chr3:191178924-191178974	Jurkat	blood:	n/a
27	chr3:191178924-191178974	PFSK-1	brain:	n/a
28	chr3:191178924-191178974	H1-hESC	embryonic stem cell:	embryo
29	chr3:191178924-191178974	K562	blood:	n/a
30	chr3:191179074-191179124	GM12878	blood:	n/a
31	chr3:191179074-191179124	IMR90	lung:	fetal
32	chr3:191178924-191178974	AG09319	gingival:	n/a
33	chr3:191178924-191178974	CMK	blood:	n/a
34	chr3:191178924-191178974	BJ	skin:	n/a
35	chr3:191178924-191178974	SK-N-SH_RA	brain:	n/a
36	chr3:191178924-191178974	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:191179074-191179124	HEEpiC	esophagus:	n/a
38	chr3:191179074-191179124	AoSMC	blood vessel:	n/a
39	chr3:191178924-191178974	SK-N-SH	brain:	n/a
40	chr3:191178924-191178974	HIPEpiC	eye:	n/a
41	chr3:191179074-191179124	H1-hESC	embryonic stem cell:	embryo
42	chr3:191179074-191179124	HRCEpiC	kidney:	n/a
43	chr3:191179074-191179124	NH-A	brain:	n/a
44	chr3:191179074-191179124	CMK	blood:	n/a
45	chr3:191179074-191179124	AG09309	skin:	n/a
46	chr3:191179074-191179124	AG10803	skin:	n/a
47	chr3:191178924-191178974	AoSMC	blood vessel:	n/a
48	chr3:191179074-191179124	GM12891	blood:	n/a
49	chr3:191179074-191179124	ECC-1	luminal epithelium:	n/a
50	chr3:191178924-191178974	MCF10A-Er-Src	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191187730..191193827-chr3:191193854..191197117,6	K562	blood:
2	chr3:191194345..191196125-chr3:191201335..191204091,2	K562	blood:
3	chr3:191160341..191162761-chr3:191179942..191182380,2	K562	blood:
4	chr3:191225876..191227408-chr3:191230738..191233284,2	K562	blood:
5	chr3:191142943..191145489-chr3:191191004..191192799,2	MCF-7	breast:
6	chr3:191161495..191163319-chr3:191214944..191216850,2	K562	blood:
7	chr3:191219513..191222335-chr3:191222361..191224281,2	MCF-7	breast:
8	chr3:191220889..191222915-chr3:191232915..191235559,2	K562	blood:
9	chr3:191210173..191212267-chr3:191228106..191229922,2	K562	blood:
10	chr3:191224872..191227257-chr3:191228159..191230428,2	K562	blood:
11	chr3:191225898..191226670-chr7:134967404..134968269,2	MCF-7	breast:
12	chr3:191150064..191152045-chr3:191218500..191220211,2	K562	blood:
13	chr3:191145766..191148014-chr3:191221969..191224844,2	K562	blood:
14	chr3:191187730..191193827-chr3:191193854..191197117,6	K562	blood:
15	chr3:191223279..191226273-chr3:191227668..191229935,2	K562	blood:
16	chr3:191144791..191146298-chr3:191179691..191181220,2	K562	blood:
17	chr3:191220446..191222407-chr3:191229444..191232369,2	K562	blood:
18	chr3:191202788..191205385-chr3:191217397..191220401,3	K562	blood:
19	chr3:191186829..191191395-chr3:191192771..191196675,4	K562	blood:
20	chr3:191220103..191221050-chr3:191527147..191528017,3	MCF-7	breast:
21	chr3:191186829..191191395-chr3:191192771..191196675,4	K562	blood:
22	chr3:191158609..191160577-chr3:191193167..191196023,2	K562	blood:
23	chr3:191144312..191145933-chr3:191218364..191220735,2	K562	blood:
24	chr3:191202788..191205385-chr3:191217397..191220401,3	K562	blood:
25	chr3:191219513..191222335-chr3:191222361..191224281,2	MCF-7	breast:
26	chr3:191194345..191196125-chr3:191201335..191204091,2	K562	blood:

No data

Variant related genes	Relation type
PYDC2	TF binding region
PYDC2	CpG island

Extended variants
information (count: 1825 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539897	chr3:191178925-191178926	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200336389	chr3:191178962-191178963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201291805	chr3:191178963-191178964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139023079	chr3:191178969-191178970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539285618	chr3:191178983-191178984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376456942	chr3:191178992-191178993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74791942	chr3:191179050-191179051	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141891926	chr3:191179074-191179075	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377321809	chr3:191179075-191179076	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376044698	chr3:191179076-191179077	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371285634	chr3:191179077-191179078	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375969173	chr3:191179078-191179079	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368331759	chr3:191179079-191179080	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199621885	chr3:191179080-191179081	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376347470	chr3:191179105-191179106	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534585157	chr3:191179115-191179116	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200714149	chr3:191179129-191179130	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554747550	chr3:191179133-191179134	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550657345	chr3:191179141-191179142	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574473285	chr3:191179156-191179157	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373113518	chr3:191179163-191179164	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199836684	chr3:191179177-191179178	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377161316	chr3:191179189-191179190	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369128849	chr3:191179192-191179193	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs293833	chr3:191179193-191179194	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs377044348	chr3:191179196-191179197	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371160069	chr3:191179203-191179204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199892707	chr3:191179216-191179217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375751040	chr3:191179247-191179248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377612256	chr3:191179269-191179270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200529665	chr3:191179276-191179277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370940837	chr3:191179277-191179278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs176823	chr3:191179303-191179304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545668053	chr3:191179332-191179333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553179135	chr3:191179459-191179460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559203767	chr3:191179511-191179512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572144844	chr3:191179602-191179603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150476599	chr3:191179623-191179624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185271267	chr3:191179625-191179626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546944738	chr3:191179642-191179643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564560	chr3:191179686-191179687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs79072813	chr3:191179718-191179719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13069775	chr3:191179721-191179722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs370811903	chr3:191179759-191179760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532576689	chr3:191179761-191179762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552940052	chr3:191179802-191179803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113957251	chr3:191179819-191179820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138311410	chr3:191179866-191179867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578004736	chr3:191179903-191179904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149618492	chr3:191179915-191179916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191175400-191190200	Weak transcription	K562	blood
2	chr3:191179000-191179200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:191179200-191179600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:191181000-191181200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:191186400-191188800	Enhancers	Fetal Lung	lung
6	chr3:191187600-191188000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr3:191187600-191188200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:191187600-191188200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:191188000-191188800	Enhancers	Fetal Muscle Leg	muscle
10	chr3:191188000-191188800	Enhancers	Ovary	ovary
11	chr3:191188800-191193400	Weak transcription	Fetal Lung	lung
12	chr3:191190200-191191400	Enhancers	K562	blood
13	chr3:191191200-191192000	Enhancers	Hela-S3	cervix
14	chr3:191191400-191191600	Flanking Active TSS	K562	blood
15	chr3:191191600-191192000	Enhancers	K562	blood
16	chr3:191192000-191192400	Weak transcription	Hela-S3	cervix
17	chr3:191192000-191193400	Weak transcription	K562	blood
18	chr3:191192400-191194800	Enhancers	Hela-S3	cervix
19	chr3:191193400-191194000	Enhancers	Fetal Lung	lung
20	chr3:191193400-191194000	Enhancers	K562	blood
21	chr3:191194000-191194400	Weak transcription	Fetal Lung	lung
22	chr3:191194000-191195000	Genic enhancers	K562	blood
23	chr3:191194200-191194800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:191194200-191194800	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr3:191194200-191195000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:191194200-191195600	Enhancers	Stomach Mucosa	stomach
27	chr3:191194400-191195000	Enhancers	Fetal Lung	lung
28	chr3:191195000-191216600	Weak transcription	K562	blood
29	chr3:191195600-191201600	Weak transcription	Stomach Mucosa	stomach
30	chr3:191198000-191201800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:191201600-191202800	Enhancers	Stomach Mucosa	stomach
32	chr3:191201800-191203200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:191202000-191202800	Enhancers	NHEK	skin
34	chr3:191202000-191203400	Enhancers	HMEC	breast
35	chr3:191202200-191202600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:191202200-191202600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:191202200-191202600	Enhancers	Hela-S3	cervix
38	chr3:191202400-191202600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:191208400-191209600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:191209200-191210000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr3:191209600-191210000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr3:191209800-191211000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:191209800-191211000	Enhancers	HMEC	breast
44	chr3:191209800-191211800	Enhancers	Fetal Lung	lung
45	chr3:191210000-191211400	Enhancers	Fetal Heart	heart
46	chr3:191210200-191210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:191210400-191210800	Enhancers	NHEK	skin
48	chr3:191211400-191216800	Weak transcription	Fetal Heart	heart
49	chr3:191211800-191217000	Weak transcription	Fetal Lung	lung
50	chr3:191216600-191217200	Enhancers	K562	blood

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