Variant report

Variant	nsv10094
Chromosome Location	chr2:97760907-97775441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr2:97764654-97764925	K562	blood:	n/a	n/a
2	CEBPB	chr2:97773446-97773645	IMR90	lung:	n/a	chr2:97773565-97773576
3	CEBPB	chr2:97773431-97773709	K562	blood:	n/a	chr2:97773565-97773576
4	CEBPB	chr2:97773440-97773636	K562	blood:	n/a	chr2:97773565-97773576
5	CEBPB	chr2:97773450-97773635	HepG2	liver:	n/a	chr2:97773565-97773576
6	CTCF	chr2:97761107-97761254	HepG2	liver:	n/a	chr2:97761161-97761174
7	CTCF	chr2:97761200-97761350	GM12870	blood:	n/a	n/a
8	CTCF	chr2:97765546-97765588	LNCaP	prostate:	n/a	n/a
9	CTCF	chr2:97761080-97761230	GM12873	blood:	n/a	chr2:97761161-97761174
10	CTCF	chr2:97763980-97764130	HepG2	liver:	n/a	n/a
11	CTCF	chr2:97761087-97761219	Pancreas_OC	pancreas:	n/a	chr2:97761161-97761174
12	CTCF	chr2:97761080-97761230	HRE	kidney:	n/a	chr2:97761161-97761174
13	CTCF	chr2:97761180-97761330	GM12864	blood:	n/a	n/a
14	CTCF	chr2:97761080-97761173	GM19238	blood:	n/a	n/a
15	CTCF	chr2:97761181-97761182	GM12878	blood:	n/a	n/a
16	CTCF	chr2:97761096-97761179	GM19239	blood:	n/a	chr2:97761161-97761174
17	CTCF	chr2:97761100-97761250	WERI-Rb-1	eye:	n/a	chr2:97761161-97761174
18	CTCF	chr2:97761101-97761163	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:97761140-97761290	GM12873	blood:	n/a	chr2:97761161-97761174
20	CTCF	chr2:97761018-97761153	GM10266	blood:	n/a	n/a
21	CTCF	chr2:97761148-97761180	Spleen_OC	spleen:	n/a	chr2:97761161-97761174
22	CTCF	chr2:97761100-97761250	Caco-2	colon:	n/a	chr2:97761161-97761174
23	CTCF	chr2:97766400-97766550	GM12866	blood:	n/a	n/a
24	CTCF	chr2:97761114-97761200	GM13977	blood:	n/a	chr2:97761161-97761174
25	CTCF	chr2:97761114-97761160	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr2:97761122-97761158	GM12892	blood:	n/a	n/a
27	CTCF	chr2:97761100-97761250	AG04449	skin:	n/a	chr2:97761161-97761174
28	CTCF	chr2:97761090-97761205	GM12891	blood:	n/a	chr2:97761161-97761174
29	CTCF	chr2:97761051-97761183	H1-hESC	embryonic stem cell:	n/a	chr2:97761161-97761174
30	CTCF	chr2:97761160-97761310	SAEC	small airway:	n/a	chr2:97761161-97761174
31	CTCF	chr2:97761071-97761214	MCF-7	breast:	n/a	chr2:97761161-97761174
32	CTCF	chr2:97761180-97761330	GM12875	blood:	n/a	n/a
33	CTCF	chr2:97761100-97761250	HCPEpiC	choroid plexus:	n/a	chr2:97761161-97761174
34	CTCF	chr2:97761140-97761290	HBMEC	blood vessel:	n/a	chr2:97761161-97761174
35	CTCF	chr2:97761160-97761310	HepG2	liver:	n/a	chr2:97761161-97761174
36	CTCF	chr2:97761121-97761126	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:97761089-97761175	NHEK	skin:	n/a	chr2:97761161-97761174
38	EBF1	chr2:97760080-97761061	GM12878	blood:	n/a	n/a
39	EBF1	chr2:97774556-97774810	GM12878	blood:	n/a	n/a
40	EBF1	chr2:97774567-97774838	GM12878	blood:	n/a	n/a
41	FOSL2	chr2:97760952-97761322	HepG2	liver:	n/a	n/a
42	FOXA1	chr2:97775000-97775442	HepG2	liver:	n/a	n/a
43	GABPA	chr2:97760730-97760951	Hela-S3	cervix:	n/a	n/a
44	HEY1	chr2:97761392-97761621	K562	blood:	n/a	n/a
45	HEY1	chr2:97759678-97761071	K562	blood:	n/a	n/a
46	HEY1	chr2:97759865-97760950	K562	blood:	n/a	n/a
47	HEY1	chr2:97760271-97761030	HepG2	liver:	n/a	n/a
48	IRF4	chr2:97760729-97761050	GM12878	blood:	n/a	n/a
49	IRF4	chr2:97760693-97761052	GM12878	blood:	n/a	n/a
50	JUND	chr2:97760895-97761167	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97761334-97761384	NHBE	bronchial:	n/a
2	chr2:97761334-97761384	SKMC	muscle:	n/a
3	chr2:97763993-97764043	NHDF-neo	bronchial:	n/a
4	chr2:97763993-97764043	Hela-S3	cervix:	n/a
5	chr2:97761334-97761384	RPTEC	kidney:	n/a
6	chr2:97763993-97764043	NH-A	brain:	n/a
7	chr2:97761354-97761404	BE2_C	brain:	n/a
8	chr2:97763993-97764043	PFSK-1	brain:	n/a
9	chr2:97761843-97761893	ovcar-3	ovarian:	n/a
10	chr2:97761843-97761893	AG09319	gingival:	n/a
11	chr2:97761843-97761893	HRPEpiC	eye:	n/a
12	chr2:97761354-97761404	SKMC	muscle:	n/a
13	chr2:97761843-97761893	A549	lung:	n/a
14	chr2:97761334-97761384	HepG2	liver:	n/a
15	chr2:97761354-97761404	Hepatocyte	liver:	n/a
16	chr2:97763993-97764043	AG10803	skin:	n/a
17	chr2:97761843-97761893	GM12891	blood:	n/a
18	chr2:97761354-97761404	Jurkat	blood:	n/a
19	chr2:97761843-97761893	NH-A	brain:	n/a
20	chr2:97761334-97761384	AG04450	lung:	fetal
21	chr2:97761354-97761404	SAEC	small airway:	n/a
22	chr2:97761843-97761893	NHDF-neo	bronchial:	n/a
23	chr2:97761334-97761384	GM06990	blood:	n/a
24	chr2:97763993-97764043	MCF10A-Er-Src	breast:	n/a
25	chr2:97761334-97761384	Caco-2	colon:	n/a
26	chr2:97761354-97761404	HIPEpiC	eye:	n/a
27	chr2:97761843-97761893	AG10803	skin:	n/a
28	chr2:97763993-97764043	HRCEpiC	kidney:	n/a
29	chr2:97763993-97764043	AG04450	lung:	fetal
30	chr2:97761354-97761404	HCT-116	colon:	n/a
31	chr2:97761354-97761404	AG04449	skin:	fetal
32	chr2:97761334-97761384	SK-N-SH_RA	brain:	n/a
33	chr2:97763993-97764043	HepG2	liver:	n/a
34	chr2:97761843-97761893	ProgFib	skin:	n/a
35	chr2:97763993-97764043	GM12891	blood:	n/a
36	chr2:97761843-97761893	HEEpiC	esophagus:	n/a
37	chr2:97761354-97761404	Hela-S3	cervix:	n/a
38	chr2:97761843-97761893	SAEC	small airway:	n/a
39	chr2:97761354-97761404	HRPEpiC	eye:	n/a
40	chr2:97763993-97764043	SKMC	muscle:	n/a
41	chr2:97761334-97761384	H1-hESC	embryonic stem cell:	embryo
42	chr2:97761334-97761384	AG04449	skin:	fetal
43	chr2:97761843-97761893	LNCaP	prostate:	n/a
44	chr2:97761354-97761404	SK-N-SH_RA	brain:	n/a
45	chr2:97761354-97761404	K562	blood:	n/a
46	chr2:97761354-97761404	HL-60	blood:	n/a
47	chr2:97763993-97764043	ECC-1	luminal epithelium:	n/a
48	chr2:97761843-97761893	T-47D	breast:	n/a
49	chr2:97761354-97761404	GM12891	blood:	n/a
50	chr2:97761354-97761404	NHBE	bronchial:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-3	chr2:97766321-97766609	NONHSAT072609

No data

Variant related genes	Relation type
FAHD2B	TF binding region
RN7SL313P	TF binding region
ANKRD36	TF binding region
FAHD2B	CpG island
RN7SL313P	CpG island
ANKRD36	CpG island

Extended variants
information (count: 128 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371437969	chr2:97761072-97761073	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs187509819	chr2:97761079-97761080	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552652796	chr2:97761104-97761105	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565041990	chr2:97761125-97761126	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs375963465	chr2:97761154-97761155	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530728215	chr2:97761181-97761182	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145494737	chr2:97761185-97761186	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs567557755	chr2:97761190-97761191	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536594406	chr2:97761212-97761213	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572047619	chr2:97761247-97761248	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs10177295	chr2:97761259-97761260	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs566479293	chr2:97761269-97761270	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs1257105	chr2:97761276-97761277	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs10177368	chr2:97761286-97761287	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191661530	chr2:97761290-97761291	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538041811	chr2:97761354-97761355	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
17	rs554791261	chr2:97761389-97761390	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs539709336	chr2:97761482-97761483	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs575008424	chr2:97761485-97761486	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs540953720	chr2:97761498-97761499	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs560250646	chr2:97761501-97761502	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs184085373	chr2:97761507-97761508	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs558004368	chr2:97761514-97761515	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs143909110	chr2:97761531-97761532	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs562979795	chr2:97761590-97761591	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs113637095	chr2:97761630-97761631	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs1257106	chr2:97761641-97761642	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs189102921	chr2:97761664-97761665	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs561101185	chr2:97761692-97761693	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs149814830	chr2:97761797-97761798	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs546895695	chr2:97761839-97761840	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs1257107	chr2:97761872-97761873	Weak transcription Enhancers Active TSS	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs542205791	chr2:97761905-97761906	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs551798760	chr2:97761912-97761913	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574074516	chr2:97761933-97761934	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs182697480	chr2:97761948-97761949	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs568610259	chr2:97761991-97761992	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537579970	chr2:97761997-97761998	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs77422608	chr2:97762052-97762053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34729549	chr2:97762053-97762054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74715923	chr2:97762071-97762072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74720762	chr2:97762076-97762077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568651656	chr2:97762081-97762082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1268684	chr2:97762107-97762108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs554448065	chr2:97762227-97762228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184425458	chr2:97762256-97762257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190456040	chr2:97762262-97762263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73961154	chr2:97762286-97762287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs115129394	chr2:97762326-97762327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181958366	chr2:97762335-97762336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97748600-97761000	Weak transcription	Primary T cells from cord blood	blood
2	chr2:97750600-97761400	Weak transcription	Lung	lung
3	chr2:97752200-97761000	Weak transcription	Fetal Kidney	kidney
4	chr2:97759400-97761200	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr2:97759600-97761000	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr2:97759600-97761000	Active TSS	Fetal Brain Female	brain
7	chr2:97759600-97761200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:97759600-97761200	Active TSS	K562	blood
9	chr2:97759800-97761000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:97759800-97761000	Active TSS	Fetal Stomach	stomach
11	chr2:97759800-97761200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:97759800-97761200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:97759800-97761200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr2:97759800-97761200	Active TSS	Stomach Smooth Muscle	stomach
15	chr2:97759800-97761200	Active TSS	A549	lung
16	chr2:97759800-97761400	Active TSS	H1 Cell Line	embryonic stem cell
17	chr2:97759800-97761400	Active TSS	H9 Cell Line	embryonic stem cell
18	chr2:97759800-97761400	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr2:97759800-97761400	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr2:97759800-97761400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:97759800-97761400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:97759800-97761600	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr2:97759800-97761600	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr2:97760000-97761000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:97760000-97761000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:97760000-97761000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr2:97760000-97761000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr2:97760000-97761000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:97760000-97761000	Active TSS	Brain Hippocampus Middle	brain
30	chr2:97760000-97761000	Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr2:97760000-97761000	Weak transcription	GM12878-XiMat	blood
32	chr2:97760000-97761200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr2:97760000-97761200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:97760000-97761400	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr2:97760000-97761400	Active TSS	Hela-S3	cervix
36	chr2:97760200-97761000	Active TSS	Dnd41	blood
37	chr2:97760400-97761000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:97760400-97761000	Active TSS	Primary B cells from peripheral blood	blood
39	chr2:97760400-97761000	Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr2:97760400-97761000	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr2:97760400-97761000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr2:97760400-97761000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:97760400-97761000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr2:97760400-97761000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:97760400-97761000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr2:97760400-97761000	Active TSS	Fetal Muscle Trunk	muscle
47	chr2:97760400-97761000	Active TSS	Left Ventricle	heart
48	chr2:97760400-97761000	Active TSS	Right Ventricle	heart
49	chr2:97760400-97761200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:97760400-97761200	Active TSS	Ovary	ovary

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