Variant report

Variant	nsv1004406
Chromosome Location	chr2:97717260-97857915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:1771)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:97778081-97778339	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:97778807-97778948	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:97778812-97778979	K562	blood:	n/a	n/a
4	ARID3A	chr2:97778120-97778444	K562	blood:	n/a	n/a
5	ATF1	chr2:97778135-97778323	K562	blood:	n/a	n/a
6	ATF1	chr2:97760434-97760794	K562	blood:	n/a	n/a
7	ATF1	chr2:97807805-97807929	K562	blood:	n/a	n/a
8	ATF3	chr2:97778756-97778914	K562	blood:	n/a	n/a
9	ATF3	chr2:97778056-97778311	GM12878	blood:	n/a	n/a
10	BACH1	chr2:97831358-97831389	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:97778797-97778986	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:97779034-97779410	GM12878	blood:	n/a	n/a
13	BATF	chr2:97759887-97760164	GM12878	blood:	n/a	n/a
14	BATF	chr2:97760489-97760619	GM12878	blood:	n/a	n/a
15	BATF	chr2:97777979-97778283	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:97778042-97778304	GM12878	blood:	n/a	chr2:97778076-97778083
17	BCL11A	chr2:97778616-97779385	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
18	BCL11A	chr2:97780056-97780285	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:97759908-97760372	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:97778704-97779122	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
21	BHLHE40	chr2:97778670-97778987	GM12878	blood:	n/a	chr2:97778882-97778898
22	BHLHE40	chr2:97778783-97778959	K562	blood:	n/a	chr2:97778882-97778898
23	BHLHE40	chr2:97778996-97779445	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:97778115-97778317	GM12878	blood:	n/a	n/a
25	BRCA1	chr2:97760435-97760807	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr2:97778112-97778312	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:97779217-97779560	Hela-S3	cervix:	n/a	chr2:97779322-97779329
28	CBX3	chr2:97760424-97760767	K562	blood:	n/a	n/a
29	CBX3	chr2:97778594-97779624	K562	blood:	n/a	n/a
30	CBX3	chr2:97779000-97779465	K562	blood:	n/a	n/a
31	CBX3	chr2:97764654-97764925	K562	blood:	n/a	n/a
32	CBX3	chr2:97778007-97778486	K562	blood:	n/a	n/a
33	CEBPB	chr2:97773450-97773635	HepG2	liver:	n/a	chr2:97773565-97773576
34	CEBPB	chr2:97773431-97773709	K562	blood:	n/a	chr2:97773565-97773576
35	CEBPB	chr2:97779104-97779603	K562	blood:	n/a	n/a
36	CEBPB	chr2:97773446-97773645	IMR90	lung:	n/a	chr2:97773565-97773576
37	CEBPB	chr2:97799578-97799766	HepG2	liver:	n/a	chr2:97799651-97799662
38	CEBPB	chr2:97778777-97779401	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:97773440-97773636	K562	blood:	n/a	chr2:97773565-97773576
40	CEBPD	chr2:97778701-97779156	K562	blood:	n/a	n/a
41	CEBPD	chr2:97778691-97779170	HepG2	liver:	n/a	n/a
42	CHD2	chr2:97778828-97779405	HepG2	liver:	n/a	chr2:97779346-97779356
43	CHD2	chr2:97778790-97779380	GM12878	blood:	n/a	chr2:97779346-97779356
44	CHD2	chr2:97778673-97779488	Hela-S3	cervix:	n/a	chr2:97779346-97779356
45	CHD2	chr2:97760599-97760634	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr2:97760524-97760708	A549	lung:	n/a	n/a
47	CREB1	chr2:97778691-97779100	A549	lung:	n/a	n/a
48	CREB1	chr2:97760530-97760694	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr2:97760499-97760714	A549	lung:	n/a	n/a
50	CTCF	chr2:97777945-97778457	H1-hESC	embryonic stem cell:	n/a	chr2:97778156-97778177 chr2:97778229-97778247 chr2:97778234-97778242 chr2:97778224-97778245 chr2:97778161-97778179 chr2:97778162-97778178

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97779411-97779461	Hela-S3	cervix:	n/a
2	chr2:97779411-97779461	HRPEpiC	eye:	n/a
3	chr2:97779411-97779461	Hela-S3	cervix:	n/a
4	chr2:97779411-97779461	HRPEpiC	eye:	n/a
5	chr2:97783139-97783189	BJ	skin:	n/a
6	chr2:97778927-97778977	IMR90	lung:	fetal
7	chr2:97760612-97760662	PrEC	prostate:	n/a
8	chr2:97779565-97779615	HAEpiC	amniotic membrane:	n/a
9	chr2:97778817-97778867	NT2-D1	testis:	n/a
10	chr2:97760726-97760776	CMK	blood:	n/a
11	chr2:97761334-97761384	IMR90	lung:	fetal
12	chr2:97779433-97779483	T-47D	breast:	n/a
13	chr2:97775474-97775524	Hepatocyte	liver:	n/a
14	chr2:97779565-97779615	SK-N-SH_RA	brain:	n/a
15	chr2:97783139-97783189	CMK	blood:	n/a
16	chr2:97775474-97775524	GM12878	blood:	n/a
17	chr2:97746622-97746672	GM06990	blood:	n/a
18	chr2:97760726-97760776	PrEC	prostate:	n/a
19	chr2:97759501-97759551	HRPEpiC	eye:	n/a
20	chr2:97778174-97778224	HMEC	breast:	n/a
21	chr2:97746622-97746672	PANC-1	pancreas:	n/a
22	chr2:97779565-97779615	Caco-2	colon:	n/a
23	chr2:97778817-97778867	HUVEC	blood vessel:	n/a
24	chr2:97760726-97760776	HEEpiC	esophagus:	n/a
25	chr2:97779565-97779615	Hela-S3	cervix:	n/a
26	chr2:97760610-97760660	BJ	skin:	n/a
27	chr2:97779433-97779483	PANC-1	pancreas:	n/a
28	chr2:97778912-97778962	ECC-1	luminal epithelium:	n/a
29	chr2:97760622-97760672	Jurkat	blood:	n/a
30	chr2:97779433-97779483	Hepatocyte	liver:	n/a
31	chr2:97760745-97760795	HNPCEpiC	eye:	n/a
32	chr2:97778912-97778962	ProgFib	skin:	n/a
33	chr2:97761334-97761384	SK-N-SH_RA	brain:	n/a
34	chr2:97761354-97761404	HepG2	liver:	n/a
35	chr2:97763993-97764043	A549	lung:	n/a
36	chr2:97756352-97756402	PFSK-1	brain:	n/a
37	chr2:97779411-97779461	HIPEpiC	eye:	n/a
38	chr2:97778927-97778977	NHBE	bronchial:	n/a
39	chr2:97761354-97761404	Jurkat	blood:	n/a
40	chr2:97779411-97779461	HepG2	liver:	n/a
41	chr2:97760612-97760662	SKMC	muscle:	n/a
42	chr2:97778817-97778867	ovcar-3	ovarian:	n/a
43	chr2:97763993-97764043	GM12878	blood:	n/a
44	chr2:97778470-97778520	H1-hESC	embryonic stem cell:	embryo
45	chr2:97759501-97759551	AG09309	skin:	n/a
46	chr2:97779519-97779569	GM12892	blood:	n/a
47	chr2:97761334-97761384	HEEpiC	esophagus:	n/a
48	chr2:97778927-97778977	LNCaP	prostate:	n/a
49	chr2:97779784-97779834	RPTEC	kidney:	n/a
50	chr2:97779784-97779834	GM06990	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:97677657..97678211-chr2:97777841..97778623,2	K562	blood:
2	chr2:97405027..97406967-chr2:97777321..97779642,2	K562	blood:
3	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
4	chr2:97522364..97524649-chr2:97747761..97749583,2	MCF-7	breast:
5	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:
6	chr2:97523665..97525724-chr2:97777402..97779360,2	MCF-7	breast:
7	chr2:97753095..97754963-chr2:97759459..97762136,2	K562	blood:
8	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:
9	chr2:97625836..97626837-chr2:97777734..97778610,3	MCF-7	breast:
10	chr2:97522570..97524502-chr2:97776940..97779479,2	MCF-7	breast:
11	chr2:97480158..97482561-chr2:97778545..97780856,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-6	chr2:97725682-97725753	NONHSAT072603
2	lnc-ANKRD36-6	chr2:97725875-97726126	NONHSAT072603
3	lnc-ANKRD36-6	chr2:97725865-97726152	NONHSAT072604
4	lnc-ANKRD36-5	chr2:97747330-97748385	NONHSAT072606
5	lnc-ANKRD36-3	chr2:97766321-97766609	NONHSAT072609

No data

Variant related genes	Relation type
IGKV1OR2-3	TF binding region
FAHD2B	TF binding region
RN7SL313P	TF binding region
ANKRD36	TF binding region
ENSG00000188383	TF binding region
IGKV1OR2-3	CpG island
FAHD2B	CpG island
RN7SL313P	CpG island
ANKRD36	CpG island
ENSG00000188383	CpG island
ENSG00000114988	chromatin interactions
ENSG00000144199	chromatin interactions
ENSG00000168763	chromatin interactions
ENSG00000213337	chromatin interactions
ENSG00000163126	chromatin interactions

Extended variants
information (count: 5040 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5040 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550499431	chr2:97717305-97717306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374747273	chr2:97717306-97717307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189351159	chr2:97717339-97717340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57668976	chr2:97717343-97717344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2707341	chr2:97717345-97717346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555558171	chr2:97717346-97717347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200986685	chr2:97717353-97717354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2443832	chr2:97717356-97717357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533940755	chr2:97717360-97717361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1257114	chr2:97717398-97717399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs577155506	chr2:97717400-97717401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569826660	chr2:97720930-97720931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535302760	chr2:97720950-97720951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548845627	chr2:97720972-97720973	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565661604	chr2:97720986-97720987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs372438622	chr2:97720999-97721000	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534286305	chr2:97721061-97721062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs557342443	chr2:97721076-97721077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577618704	chr2:97721080-97721081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537148156	chr2:97721090-97721091	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs1257077	chr2:97721091-97721092	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
22	rs1257076	chr2:97721106-97721107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
23	rs559178687	chr2:97721981-97721982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs538409853	chr2:97721989-97721990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs75447135	chr2:97721990-97721991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs112027519	chr2:97722045-97722046	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556294118	chr2:97722103-97722104	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs554669534	chr2:97722109-97722110	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs113628884	chr2:97722137-97722138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs574541537	chr2:97722152-97722153	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs540320811	chr2:97722207-97722208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs553814444	chr2:97722666-97722667	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs577276094	chr2:97722667-97722668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs189929734	chr2:97722673-97722674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564926715	chr2:97722719-97722720	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs370343138	chr2:97722745-97722746	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575434320	chr2:97722748-97722749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs552295637	chr2:97723094-97723095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs368739152	chr2:97723127-97723128	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs79731542	chr2:97723141-97723142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs569343760	chr2:97723169-97723170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs2707337	chr2:97723182-97723183	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2950994	chr2:97723614-97723615	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs9711395	chr2:97723640-97723641	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs2314846	chr2:97723673-97723674	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577212608	chr2:97723692-97723693	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs2314845	chr2:97723701-97723702	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539538840	chr2:97723710-97723711	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs556650291	chr2:97723717-97723718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74411970	chr2:97723720-97723721	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1192 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97710400-97717400	Enhancers	Primary B cells from peripheral blood	blood
2	chr2:97723600-97723800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:97724600-97724800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:97724600-97724800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:97724600-97724800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:97724800-97725800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr2:97725400-97726200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:97725800-97726200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:97725800-97726200	Enhancers	Ovary	ovary
10	chr2:97731800-97732200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:97732000-97732200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:97732200-97733200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:97732200-97733400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:97732600-97734800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:97733200-97733800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:97733200-97734000	ZNF genes & repeats	Gastric	stomach
17	chr2:97733200-97734200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:97733400-97733800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
19	chr2:97733400-97734000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:97733400-97734000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:97733600-97733800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
22	chr2:97733600-97734000	Enhancers	Brain Germinal Matrix	brain
23	chr2:97733800-97734000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:97733800-97734200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:97734200-97738600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:97738600-97738800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:97744800-97745000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:97745000-97760600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:97746600-97759800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr2:97747000-97760600	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:97747200-97760800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr2:97747400-97749200	Weak transcription	Fetal Stomach	stomach
33	chr2:97747600-97748600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr2:97747600-97749600	Enhancers	Esophagus	oesophagus
35	chr2:97747600-97759800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr2:97747800-97748000	Enhancers	Brain Hippocampus Middle	brain
37	chr2:97748000-97749400	Weak transcription	Brain Hippocampus Middle	brain
38	chr2:97748000-97759800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr2:97748000-97760400	Weak transcription	Ovary	ovary
40	chr2:97748000-97760400	Weak transcription	Right Ventricle	heart
41	chr2:97748000-97760600	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr2:97748000-97760800	Weak transcription	Brain Substantia Nigra	brain
43	chr2:97748600-97756200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr2:97748600-97760800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr2:97748600-97761000	Weak transcription	Primary T cells from cord blood	blood
46	chr2:97748800-97760600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr2:97749200-97750800	Strong transcription	Fetal Stomach	stomach
48	chr2:97749400-97750200	Strong transcription	Brain Hippocampus Middle	brain
49	chr2:97749800-97759600	Weak transcription	Fetal Brain Female	brain
50	chr2:97750200-97758800	Weak transcription	Brain Hippocampus Middle	brain

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