Variant report

Variant	nsv875721
Chromosome Location	chr2:205232072-205306024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:299)
CpG islands
(count:123)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:205271921-205272766	K562	blood:	n/a	n/a
2	ARID3A	chr2:205299440-205300061	K562	blood:	n/a	n/a
3	ARID3A	chr2:205237651-205237662	K562	blood:	n/a	n/a
4	ARID3A	chr2:205273015-205274002	K562	blood:	n/a	chr2:205273232-205273248
5	ARID3A	chr2:205272474-205272805	HepG2	liver:	n/a	n/a
6	ATF1	chr2:205293328-205293528	K562	blood:	n/a	n/a
7	BHLHE40	chr2:205302841-205303245	HepG2	liver:	n/a	n/a
8	BHLHE40	chr2:205244908-205245142	HepG2	liver:	n/a	n/a
9	BHLHE40	chr2:205272362-205272757	K562	blood:	n/a	n/a
10	BHLHE40	chr2:205272441-205272658	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:205237331-205237545	K562	blood:	n/a	chr2:205237422-205237431 chr2:205237422-205237431 chr2:205237421-205237430 chr2:205237416-205237437
12	BHLHE40	chr2:205299491-205299727	K562	blood:	n/a	n/a
13	BHLHE40	chr2:205244926-205245094	K562	blood:	n/a	n/a
14	CBX3	chr2:205277502-205277905	K562	blood:	n/a	n/a
15	CBX3	chr2:205277553-205277797	K562	blood:	n/a	n/a
16	CBX3	chr2:205278645-205278931	K562	blood:	n/a	n/a
17	CBX3	chr2:205296931-205297312	K562	blood:	n/a	n/a
18	CBX3	chr2:205272424-205272710	K562	blood:	n/a	n/a
19	CCNT2	chr2:205272453-205272743	K562	blood:	n/a	n/a
20	CCNT2	chr2:205273434-205273873	K562	blood:	n/a	chr2:205273478-205273487
21	CCNT2	chr2:205299235-205299940	K562	blood:	n/a	n/a
22	CEBPB	chr2:205253497-205253536	HepG2	liver:	n/a	chr2:205253510-205253521 chr2:205253507-205253524
23	CEBPB	chr2:205237115-205237164	K562	blood:	n/a	n/a
24	CEBPB	chr2:205272113-205272787	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:205272412-205272785	K562	blood:	n/a	n/a
26	CEBPB	chr2:205272409-205272752	K562	blood:	n/a	n/a
27	CEBPB	chr2:205237019-205237175	HepG2	liver:	n/a	n/a
28	CEBPD	chr2:205272507-205272823	K562	blood:	n/a	n/a
29	CEBPD	chr2:205299369-205299921	K562	blood:	n/a	n/a
30	CEBPD	chr2:205272360-205272794	K562	blood:	n/a	n/a
31	CHD2	chr2:205245275-205245388	GM12878	blood:	n/a	n/a
32	CTCF	chr2:205293552-205293643	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:205293680-205293830	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr2:205299432-205299646	K562	blood:	n/a	n/a
35	CTCF	chr2:205293480-205293630	A549	lung:	n/a	n/a
36	CTCF	chr2:205232320-205232470	NHLF	lung:	n/a	n/a
37	CTCF	chr2:205293500-205293650	AG04449	skin:	n/a	n/a
38	CTCF	chr2:205247460-205247519	GM20000	blood:	n/a	n/a
39	CTCF	chr2:205293520-205293670	HEK293	kidney:	n/a	n/a
40	CTCF	chr2:205293520-205293670	HCFaa	heart:	n/a	n/a
41	CTCF	chr2:205293573-205293635	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:205293540-205293690	HAc	cerebellar:	n/a	n/a
43	CTCF	chr2:205293480-205293630	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr2:205293598-205293656	HepG2	liver:	n/a	n/a
45	CTCF	chr2:205293520-205293670	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr2:205293440-205293590	A549	lung:	n/a	n/a
47	CTCF	chr2:205300571-205300776	K562	blood:	n/a	n/a
48	CTCF	chr2:205293565-205293634	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:205293538-205293679	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:205293580-205293730	AG09319	gingival:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:205234408-205234458	PANC-1	pancreas:	n/a
2	chr2:205234408-205234458	PANC-1	pancreas:	n/a
3	chr2:205234408-205234458	HL-60	blood:	n/a
4	chr2:205303100-205303150	PFSK-1	brain:	n/a
5	chr2:205234408-205234458	LNCaP	prostate:	n/a
6	chr2:205234408-205234458	ProgFib	skin:	n/a
7	chr2:205234408-205234458	AG04449	skin:	fetal
8	chr2:205234408-205234458	NT2-D1	testis:	n/a
9	chr2:205234408-205234458	T-47D	breast:	n/a
10	chr2:205303100-205303150	ECC-1	luminal epithelium:	n/a
11	chr2:205234408-205234458	H1-hESC	embryonic stem cell:	embryo
12	chr2:205234408-205234458	HRPEpiC	eye:	n/a
13	chr2:205303100-205303150	SK-N-MC	brain:	n/a
14	chr2:205234408-205234458	SAEC	small airway:	n/a
15	chr2:205234408-205234458	AG09319	gingival:	n/a
16	chr2:205303100-205303150	PrEC	prostate:	n/a
17	chr2:205234408-205234458	K562	blood:	n/a
18	chr2:205234408-205234458	U87	brain:	n/a
19	chr2:205303100-205303150	Caco-2	colon:	n/a
20	chr2:205234408-205234458	HCM	heart:	n/a
21	chr2:205303100-205303150	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:205303100-205303150	Hela-S3	cervix:	n/a
23	chr2:205234408-205234458	PFSK-1	brain:	n/a
24	chr2:205234408-205234458	GM19239	blood:	n/a
25	chr2:205303100-205303150	IMR90	lung:	fetal
26	chr2:205303100-205303150	CMK	blood:	n/a
27	chr2:205303100-205303150	A549	lung:	n/a
28	chr2:205234408-205234458	AG09309	skin:	n/a
29	chr2:205234408-205234458	GM12892	blood:	n/a
30	chr2:205303100-205303150	NB4	blood:	n/a
31	chr2:205234408-205234458	HCT-116	colon:	n/a
32	chr2:205234408-205234458	HepG2	liver:	n/a
33	chr2:205234408-205234458	AG04450	lung:	fetal
34	chr2:205234408-205234458	HIPEpiC	eye:	n/a
35	chr2:205303100-205303150	HL-60	blood:	n/a
36	chr2:205234408-205234458	Caco-2	colon:	n/a
37	chr2:205234408-205234458	Hela-S3	cervix:	n/a
38	chr2:205234408-205234458	BE2_C	brain:	n/a
39	chr2:205234408-205234458	SK-N-SH	brain:	n/a
40	chr2:205303100-205303150	BJ	skin:	n/a
41	chr2:205234408-205234458	NH-A	brain:	n/a
42	chr2:205234408-205234458	A549	lung:	n/a
43	chr2:205303100-205303150	HIPEpiC	eye:	n/a
44	chr2:205303100-205303150	NHBE	bronchial:	n/a
45	chr2:205303100-205303150	SAEC	small airway:	n/a
46	chr2:205303100-205303150	HEK293	kidney:	embryo
47	chr2:205234408-205234458	SK-N-MC	brain:	n/a
48	chr2:205303100-205303150	AoSMC	blood vessel:	n/a
49	chr2:205303100-205303150	GM19239	blood:	n/a
50	chr2:205234408-205234458	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:205237902..205239456-chr2:205244157..205245908,2	MCF-7	breast:
2	chr2:205258775..205261159-chr2:205262686..205264386,2	K562	blood:
3	chr2:205268926..205271730-chr2:205279603..205282127,2	K562	blood:
4	chr2:205266083..205268552-chr2:205270043..205272766,3	K562	blood:
5	chr2:205237902..205239456-chr2:205244157..205245908,2	MCF-7	breast:
6	chr2:205267017..205269993-chr2:205273043..205275559,2	K562	blood:
7	chr2:205262660..205264266-chr2:205270395..205272179,2	K562	blood:
8	chr2:205266083..205268552-chr2:205270043..205272766,3	K562	blood:
9	chr2:205298407..205299915-chr2:205301939..205303492,2	K562	blood:
10	chr2:205267017..205269993-chr2:205273043..205275559,2	K562	blood:
11	chr2:205266871..205268427-chr2:205270043..205271674,2	K562	blood:
12	chr2:205298407..205299915-chr2:205301939..205303492,2	K562	blood:
13	chr2:205258775..205261159-chr2:205262686..205264386,2	K562	blood:
14	chr2:205269954..205272543-chr2:205315221..205317326,2	K562	blood:
15	chr2:205266871..205268427-chr2:205270043..205271674,2	K562	blood:
16	chr2:205262660..205264266-chr2:205270395..205272179,2	K562	blood:
17	chr2:205292640..205295418-chr2:205371995..205374961,2	K562	blood:
18	chr2:205223246..205226106-chr2:205231511..205234500,2	MCF-7	breast:
19	chr2:205297634..205300011-chr2:205411567..205413627,2	K562	blood:
20	chr2:205227423..205230387-chr2:205244483..205246594,2	K562	blood:
21	chr2:205268926..205271730-chr2:205279603..205282127,2	K562	blood:
22	chr2:204979465..204980271-chr2:205272464..205273025,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARD3B-5	chr2:205243818-205244515	NONHSAT076505

No data

Variant related genes	Relation type
ENSG00000225304	TF binding region
ENSG00000225304	CpG island

Extended variants
information (count: 1331 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13035221	chr2:205232072-205232073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374085708	chr2:205232110-205232111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72930619	chr2:205232155-205232156	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs141306574	chr2:205232189-205232190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570135663	chr2:205232203-205232204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553394016	chr2:205232263-205232264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149817588	chr2:205232319-205232320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7581860	chr2:205232320-205232321	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs370846580	chr2:205232396-205232397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189553848	chr2:205232407-205232408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145816203	chr2:205232463-205232464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180786832	chr2:205232494-205232495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577987998	chr2:205232508-205232509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542391847	chr2:205232537-205232538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545139378	chr2:205232565-205232566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114970480	chr2:205232577-205232578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545366835	chr2:205232578-205232579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148997204	chr2:205232585-205232586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7608404	chr2:205232597-205232598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143814631	chr2:205232645-205232646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185452311	chr2:205232670-205232671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188646481	chr2:205232690-205232691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564691523	chr2:205232698-205232699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148180060	chr2:205232726-205232727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141943305	chr2:205232777-205232778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181091032	chr2:205232778-205232779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568980809	chr2:205232779-205232780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542775902	chr2:205232795-205232796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531000475	chr2:205232856-205232857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186593225	chr2:205232863-205232864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191441682	chr2:205232912-205232913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73982215	chr2:205232967-205232968	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs183758727	chr2:205233019-205233020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13398807	chr2:205233022-205233023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560928352	chr2:205233049-205233050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528099457	chr2:205233069-205233070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546536945	chr2:205233070-205233071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539067397	chr2:205233095-205233096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186158905	chr2:205233108-205233109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370393685	chr2:205233116-205233117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543147312	chr2:205233121-205233122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375680242	chr2:205233143-205233144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145781918	chr2:205233200-205233201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191013911	chr2:205233217-205233218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577858795	chr2:205233234-205233235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141760757	chr2:205233235-205233236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540517186	chr2:205233285-205233286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562476764	chr2:205233326-205233327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138705691	chr2:205233349-205233350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544236855	chr2:205233405-205233406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Intracranial aneurysm	16715129	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205229800-205238600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:205230200-205234800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:205230800-205234000	Weak transcription	Fetal Kidney	kidney
4	chr2:205231000-205233600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:205231000-205234200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:205231200-205234600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:205232000-205233200	Enhancers	Fetal Lung	lung
8	chr2:205232400-205232600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:205232800-205234400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:205233000-205233200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:205233000-205233200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:205233000-205233200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:205233000-205233200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:205233200-205234400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:205233200-205234400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr2:205233200-205234400	Weak transcription	Fetal Lung	lung
17	chr2:205233200-205234800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:205233400-205234600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:205233600-205236800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:205233800-205235200	Enhancers	Brain Germinal Matrix	brain
21	chr2:205234000-205234200	Enhancers	Fetal Kidney	kidney
22	chr2:205234000-205235600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:205234200-205235000	Weak transcription	Fetal Kidney	kidney
24	chr2:205234200-205235800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:205234400-205235400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr2:205234400-205235400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:205234400-205235400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:205234400-205235400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:205234400-205235400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:205234400-205235400	Enhancers	Fetal Lung	lung
31	chr2:205234600-205235400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:205234600-205235400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr2:205234800-205235200	Enhancers	Fetal Brain Male	brain
34	chr2:205234800-205235400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:205234800-205235400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:205234800-205235400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:205234800-205235600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:205234800-205235600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr2:205235000-205235200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:205235000-205235400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr2:205235000-205235400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr2:205235000-205235400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:205235000-205235400	Enhancers	Fetal Kidney	kidney
44	chr2:205235200-205236400	Weak transcription	Brain Germinal Matrix	brain
45	chr2:205235400-205236400	Weak transcription	Fetal Lung	lung
46	chr2:205236600-205236800	Enhancers	Brain Germinal Matrix	brain
47	chr2:205236600-205236800	Enhancers	Fetal Lung	lung
48	chr2:205238600-205239000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:205252800-205254200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr2:205253400-205253800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links