Variant report

Variant	nsv1004291
Chromosome Location	chr2:99855978-99919999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99870939-99870988	K562	blood:	n/a	n/a
2	ARID3A	chr2:99895164-99895764	HepG2	liver:	n/a	n/a
3	BATF	chr2:99856950-99857204	GM12878	blood:	n/a	n/a
4	BATF	chr2:99856972-99857225	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
7	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
9	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
10	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
11	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
12	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
13	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
15	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
20	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
21	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
24	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
25	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
26	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
27	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
28	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
29	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
30	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
31	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
32	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
33	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
34	CTCF	chr2:99862560-99862710	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:99862520-99862670	GM12868	blood:	n/a	n/a
36	CTCF	chr2:99862140-99862290	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:99855860-99856010	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr2:99856000-99856150	HAc	cerebellar:	n/a	n/a
39	CTCF	chr2:99862210-99862311	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:99862180-99862330	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:99862580-99862730	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:99855920-99856070	GM12864	blood:	n/a	n/a
43	CTCF	chr2:99863180-99863330	HepG2	liver:	n/a	n/a
44	CTCF	chr2:99862520-99862670	SAEC	small airway:	n/a	n/a
45	CTCF	chr2:99862183-99862352	HepG2	liver:	n/a	n/a
46	CTCF	chr2:99855880-99856030	HL-60	blood:	n/a	n/a
47	CTCF	chr2:99855900-99856050	AG04450	lung:	n/a	n/a
48	CTCF	chr2:99862580-99862730	HL-60	blood:	n/a	n/a
49	CTCF	chr2:99862129-99862414	HepG2	liver:	n/a	n/a
50	CTCF	chr2:99862560-99862710	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99872119-99872169	ProgFib	skin:	n/a
2	chr2:99918603-99918653	SK-N-MC	brain:	n/a
3	chr2:99872119-99872169	SK-N-SH_RA	brain:	n/a
4	chr2:99918042-99918092	HCT-116	colon:	n/a
5	chr2:99908962-99909012	Jurkat	blood:	n/a
6	chr2:99918767-99918817	SK-N-SH	brain:	n/a
7	chr2:99871270-99871320	CMK	blood:	n/a
8	chr2:99917669-99917719	HCM	heart:	n/a
9	chr2:99918664-99918714	SK-N-SH	brain:	n/a
10	chr2:99918603-99918653	HMEC	breast:	n/a
11	chr2:99912152-99912202	SKMC	muscle:	n/a
12	chr2:99918042-99918092	PFSK-1	brain:	n/a
13	chr2:99872119-99872169	IMR90	lung:	fetal
14	chr2:99871270-99871320	U87	brain:	n/a
15	chr2:99908962-99909012	AG09309	skin:	n/a
16	chr2:99908962-99909012	Hela-S3	cervix:	n/a
17	chr2:99871575-99871625	AoSMC	blood vessel:	n/a
18	chr2:99908962-99909012	GM12892	blood:	n/a
19	chr2:99871988-99872038	Hepatocyte	liver:	n/a
20	chr2:99918664-99918714	Caco-2	colon:	n/a
21	chr2:99867344-99867394	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:99871988-99872038	AoSMC	blood vessel:	n/a
23	chr2:99912152-99912202	SK-N-SH	brain:	n/a
24	chr2:99918603-99918653	GM06990	blood:	n/a
25	chr2:99867344-99867394	SAEC	small airway:	n/a
26	chr2:99872119-99872169	HCF	heart:	n/a
27	chr2:99918664-99918714	Hepatocyte	liver:	n/a
28	chr2:99858763-99858813	SK-N-MC	brain:	n/a
29	chr2:99871575-99871625	AG10803	skin:	n/a
30	chr2:99867344-99867394	LNCaP	prostate:	n/a
31	chr2:99912152-99912202	ovcar-3	ovarian:	n/a
32	chr2:99912152-99912202	ECC-1	luminal epithelium:	n/a
33	chr2:99871738-99871788	PANC-1	pancreas:	n/a
34	chr2:99908962-99909012	HAEpiC	amniotic membrane:	n/a
35	chr2:99918603-99918653	LNCaP	prostate:	n/a
36	chr2:99918767-99918817	Caco-2	colon:	n/a
37	chr2:99918042-99918092	PrEC	prostate:	n/a
38	chr2:99858763-99858813	T-47D	breast:	n/a
39	chr2:99918664-99918714	PANC-1	pancreas:	n/a
40	chr2:99918767-99918817	T-47D	breast:	n/a
41	chr2:99871738-99871788	ovcar-3	ovarian:	n/a
42	chr2:99918603-99918653	HEK293	kidney:	embryo
43	chr2:99871270-99871320	PrEC	prostate:	n/a
44	chr2:99871738-99871788	A549	lung:	n/a
45	chr2:99871738-99871788	NB4	blood:	n/a
46	chr2:99918042-99918092	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:99871738-99871788	Caco-2	colon:	n/a
48	chr2:99871738-99871788	Hepatocyte	liver:	n/a
49	chr2:99871270-99871320	HCPEpiC	choroid plexus:	n/a
50	chr2:99871270-99871320	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
2	chr2:99918821..99920555-chr2:99920714..99922754,2	MCF-7	breast:
3	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
4	chr2:99795164..99797878-chr2:99854234..99856098,2	K562	blood:
5	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
6	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
7	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
8	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
9	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
10	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
11	chr2:99919697..99922118-chr2:99951528..99953553,2	K562	blood:
12	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
13	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
14	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
15	chr2:99855888..99858243-chr2:99952048..99955134,3	MCF-7	breast:
16	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
17	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
18	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:

Variant related genes	Relation type
LYG2	TF binding region
C2orf15	TF binding region
LYG1	TF binding region
LYG2	CpG island
C2orf15	CpG island
LYG1	CpG island
ENSG00000158411	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000144214	chromatin interactions
ENSG00000185414	chromatin interactions

Extended variants
information (count: 2217 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2217 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561534163	chr2:99855985-99855986	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs530314705	chr2:99856005-99856006	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs567752844	chr2:99856092-99856093	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs535158377	chr2:99856120-99856121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547301911	chr2:99856130-99856131	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs376486856	chr2:99856135-99856136	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs538635539	chr2:99856144-99856145	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551936150	chr2:99856201-99856202	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs71413821	chr2:99856226-99856227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs70940155	chr2:99856227-99856228	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374497758	chr2:99856246-99856247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568630638	chr2:99856267-99856268	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs188780730	chr2:99856315-99856316	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs542461123	chr2:99856346-99856347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554327184	chr2:99856347-99856348	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs13022798	chr2:99856378-99856379	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs372147807	chr2:99856401-99856402	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs533842332	chr2:99856402-99856403	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75269256	chr2:99856489-99856490	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573114634	chr2:99856555-99856556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs192162069	chr2:99856561-99856562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545388803	chr2:99856593-99856594	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183488260	chr2:99856594-99856595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs575826171	chr2:99856639-99856640	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188795102	chr2:99856662-99856663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs192063427	chr2:99856702-99856703	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557776669	chr2:99856729-99856730	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572836647	chr2:99856804-99856805	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184333991	chr2:99856885-99856886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142722185	chr2:99856919-99856920	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147424822	chr2:99856976-99856977	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373247664	chr2:99856996-99856997	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531981974	chr2:99857002-99857003	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139799681	chr2:99857052-99857053	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs568547139	chr2:99857069-99857070	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs74661138	chr2:99857100-99857101	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs372493084	chr2:99857114-99857115	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs547928180	chr2:99857138-99857139	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568154191	chr2:99857143-99857144	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187126522	chr2:99857178-99857179	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543962204	chr2:99857240-99857241	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs145303854	chr2:99857257-99857258	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570746262	chr2:99857276-99857277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191469547	chr2:99857322-99857323	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184259839	chr2:99857346-99857347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs75340268	chr2:99857353-99857354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544716487	chr2:99857430-99857431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555107973	chr2:99857499-99857500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs377319274	chr2:99857636-99857637	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574886399	chr2:99857650-99857651	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99840800-99874400	Weak transcription	Aorta	Aorta
2	chr2:99853600-99863200	Weak transcription	Esophagus	oesophagus
3	chr2:99854800-99865800	Weak transcription	Left Ventricle	heart
4	chr2:99858200-99859200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:99858400-99859200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:99858800-99864800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:99860400-99899800	Weak transcription	Psoas Muscle	Psoas
8	chr2:99860800-99864400	Weak transcription	Lung	lung
9	chr2:99861200-99879200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr2:99861200-99900800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:99861800-99871200	Weak transcription	Colon Smooth Muscle	Colon
12	chr2:99861800-99899400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:99862000-99863600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:99862000-99879200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr2:99862200-99864200	Enhancers	HepG2	liver
16	chr2:99862600-99863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:99863000-99863400	Enhancers	Gastric	stomach
18	chr2:99863200-99863400	ZNF genes & repeats	Esophagus	oesophagus
19	chr2:99864200-99867200	Weak transcription	HepG2	liver
20	chr2:99867200-99867400	Enhancers	HepG2	liver
21	chr2:99867200-99867600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:99869800-99880000	Weak transcription	Right Ventricle	heart
23	chr2:99870600-99871200	Enhancers	Stomach Mucosa	stomach
24	chr2:99872000-99872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:99872000-99873200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr2:99872000-99873800	Enhancers	HMEC	breast
27	chr2:99872200-99872400	Bivalent Enhancer	HepG2	liver
28	chr2:99872200-99872600	Enhancers	NHEK	skin
29	chr2:99872200-99872800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:99872200-99873000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:99872200-99873600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:99872400-99872800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:99872400-99873000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:99872400-99873000	Enhancers	Esophagus	oesophagus
35	chr2:99872400-99873200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:99872400-99873600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:99872600-99873000	Flanking Active TSS	NHEK	skin
38	chr2:99872600-99873200	Enhancers	NH-A	brain
39	chr2:99872800-99873200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:99872800-99873400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:99873000-99873800	Enhancers	NHEK	skin
42	chr2:99873000-99877600	Weak transcription	Esophagus	oesophagus
43	chr2:99873200-99875600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:99873400-99877600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:99873600-99877800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:99873800-99877600	Weak transcription	HMEC	breast
47	chr2:99873800-99900600	Weak transcription	Ovary	ovary
48	chr2:99874400-99874600	ZNF genes & repeats	Aorta	Aorta
49	chr2:99874600-99879400	Weak transcription	Aorta	Aorta
50	chr2:99876200-99882400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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