Variant report

Variant	esv1845945
Chromosome Location	chr2:97859833-98202258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1368)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:160)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:97899391-97899606	GM12878	blood:	n/a	n/a
2	BATF	chr2:97942120-97942451	GM12878	blood:	n/a	n/a
3	BATF	chr2:98096813-98097157	GM12878	blood:	n/a	n/a
4	BATF	chr2:98137602-98137837	GM12878	blood:	n/a	n/a
5	BATF	chr2:97873792-97873985	GM12878	blood:	n/a	n/a
6	BATF	chr2:98194694-98194913	GM12878	blood:	n/a	n/a
7	BATF	chr2:97942129-97942430	GM12878	blood:	n/a	n/a
8	BATF	chr2:98158810-98158993	GM12878	blood:	n/a	n/a
9	BATF	chr2:97913986-97914232	GM12878	blood:	n/a	n/a
10	BATF	chr2:98096792-98097131	GM12878	blood:	n/a	n/a
11	BATF	chr2:98139756-98139918	GM12878	blood:	n/a	n/a
12	BATF	chr2:97880580-97880763	GM12878	blood:	n/a	n/a
13	BATF	chr2:97901525-97901760	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:97899417-97899668	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:98132740-98132967	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:98139694-98139945	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:97873717-97873957	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:97869663-97870214	HepG2	liver:	n/a	n/a
19	BHLHE40	chr2:97906395-97906622	HepG2	liver:	n/a	n/a
20	CBX3	chr2:97896489-97896815	K562	blood:	n/a	n/a
21	CEBPB	chr2:98019815-98020123	A549	lung:	n/a	chr2:98019886-98019897
22	CEBPB	chr2:98018246-98018416	A549	lung:	n/a	n/a
23	CEBPB	chr2:97877884-97877967	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:98018225-98018551	HepG2	liver:	n/a	n/a
25	CHD2	chr2:98025044-98025343	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:98017540-98017690	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr2:98017560-98017710	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:97971376-97971420	H1-hESC	embryonic stem cell:	n/a	chr2:97971405-97971414
29	CTCF	chr2:98017510-98017774	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:98017260-98017410	GM12870	blood:	n/a	n/a
31	CTCF	chr2:98068003-98068109	ProgFib	skin:	n/a	chr2:98068023-98068041
32	CTCF	chr2:98137517-98137596	Medullo	brain:	n/a	n/a
33	CTCF	chr2:98017440-98017746	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr2:98068002-98068068	GM10266	blood:	n/a	chr2:98068023-98068041
35	CTCF	chr2:97970796-97970917	GM13977	blood:	n/a	chr2:97970855-97970873
36	CTCF	chr2:98017540-98017690	BE2_C	brain:	n/a	n/a
37	CTCF	chr2:98150167-98150228	GM13977	blood:	n/a	n/a
38	CTCF	chr2:98067937-98068151	Gliobla	brain:	n/a	chr2:98068023-98068041
39	CTCF	chr2:97996509-97996532	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr2:97970717-97970972	LNCaP	prostate:	n/a	chr2:97970855-97970873
41	CTCF	chr2:98067948-98068152	MCF-7	breast:	n/a	chr2:98068023-98068041
42	CTCF	chr2:98071602-98071693	GM13976	blood:	n/a	n/a
43	CTCF	chr2:98068002-98068090	GM19240	blood:	n/a	chr2:98068023-98068041
44	CTCF	chr2:97976204-97976310	Medullo	brain:	n/a	n/a
45	CTCF	chr2:98111843-98111868	Medullo	brain:	n/a	n/a
46	CTCF	chr2:98165380-98165530	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr2:98067956-98068095	Hela-S3	cervix:	n/a	chr2:98068023-98068041
48	CTCF	chr2:98166292-98166313	GM20000	blood:	n/a	n/a
49	CTCF	chr2:97883253-97883274	GM10248	blood:	n/a	n/a
50	CTCF	chr2:98017545-98017724	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:98012288..98014989-chr2:98016179..98017699,2	MCF-7	breast:
2	chr11:65274173..65274684-chr2:98182548..98183048,2	Hela-S3	cervix:
3	chr2:98019789..98021903-chr2:98023774..98026481,2	MCF-7	breast:
4	chr2:98013225..98016520-chr2:98024524..98026822,3	MCF-7	breast:
5	chr2:98021214..98022721-chr2:98024555..98026401,2	K562	blood:
6	chr2:98012288..98014989-chr2:98016179..98017699,2	MCF-7	breast:
7	chr2:98013205..98013710-chr2:98025264..98025790,2	MCF-7	breast:
8	chr2:98015115..98017129-chr2:98018538..98021537,2	K562	blood:
9	chr2:98201716..98203846-chr2:98280440..98282039,2	K562	blood:
10	chr2:98013205..98013710-chr2:98025264..98025790,2	MCF-7	breast:
11	chr2:97866538..97868238-chr3:73158384..73160590,2	MCF-7	breast:

(count:160 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTR1B-3	chr2:98081774-98082014	ENSG00000230606.6
2	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072636
3	lnc-ACTR1B-6	chr2:98140412-98141439	NONHSAT072652
4	lnc-ACTR1B-2	chr2:98104342-98104688	XLOC_002219
5	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
6	lnc-FAHD2B-3	chr2:97935204-97935466	XLOC_002215
7	lnc-ACTR1B-3	chr2:98081676-98082014	NONHSAT072631
8	lnc-ACTR1B-9	chr2:98024520-98024800	NONHSAT072625
9	lnc-ACTR1B-3	chr2:98089391-98089511	ENSG00000230606.6
10	lnc-ACTR1B-3	chr2:98089888-98089998	ENSG00000230606.6
11	lnc-ANKRD36-1	chr2:97950615-97950744	XLOC_001583
12	lnc-FAHD2B-1	chr2:97932290-97932416	XLOC_002214
13	lnc-ANKRD36-2	chr2:98088553-98088902	ENSG00000241481.2
14	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606
15	lnc-ACTR1B-3	chr2:98088770-98088849	ENSG00000230606
16	lnc-ACTR1B-3	chr2:98081812-98082014	ENSG00000230606.6
17	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
18	lnc-ANKRD36-1	chr2:97951040-97951260	XLOC_001583
19	lnc-ACTR1B-1	chr2:98105261-98105300	XLOC_002220
20	lnc-ACTR1B-3	chr2:98088770-98090673	NONHSAT072638
21	lnc-ANKRD36-11	chr2:98041867-98042166	NONHSAT072627
22	lnc-ACTR1B-3	chr2:98088032-98088252	ENSG00000230606.6
23	lnc-ACTR1B-3	chr2:98081083-98082014	ENSG00000230606.6
24	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072642
25	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606
26	lnc-ACTR1B-3	chr2:98088770-98088854	ENSG00000230606.6
27	lnc-ACTR1B-3	chr2:98088770-98088865	NONHSAT072631
28	lnc-ACTR1B-3	chr2:98088032-98088090	ENSG00000230606.6
29	lnc-ACTR1B-3	chr2:98094797-98094824	NONHSAT072631
30	lnc-ACTR1B-3	chr2:98088770-98091049	ENSG00000230606.6
31	lnc-FAHD2B-2	chr2:97932879-97933133	XLOC_002216
32	lnc-ACTR1B-3	chr2:98088770-98089122	ENSG00000230606
33	lnc-ACTR1B-3	chr2:98081676-98082014	NR_040097
34	lnc-ACTR1B-1	chr2:98104748-98105157	XLOC_002220
35	lnc-FAHD2B-1	chr2:97933186-97933205	XLOC_002214
36	lnc-ACTR1B-3	chr2:98088173-98088252	ENSG00000230606.6
37	lnc-ACTR1B-3	chr2:98088519-98088677	NONHSAT072644
38	lnc-ANKRD36-1	chr2:97948301-97950522	NONHSAT072617
39	lnc-ACTR1B-3	chr2:98081922-98082014	ENSG00000230606.6
40	lnc-FAHD2B-1	chr2:97933309-97933708	XLOC_002214
41	lnc-ACTR1B-3	chr2:98088770-98090529	NONHSAT072644
42	lnc-ACTR1B-4	chr2:98071668-98071970	XLOC_002217
43	lnc-ACTR1B-3	chr2:98089395-98089994	ENSG00000230606.6
44	lnc-ANKRD36-1	chr2:97950615-97950744	NONHSAT072620
45	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606.6
46	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606
47	lnc-ANKRD36-2	chr2:98086678-98086841	XLOC_001584
48	lnc-ACTR1B-8	chr2:98123499-98123528	NONHSAT072651
49	lnc-ANKRD36-1	chr2:97950615-97950744	NONHSAT072617
50	lnc-ACTR1B-3	chr2:98089382-98089511	ENSG00000230606.6

No data

Variant related genes	Relation type
ANKRD36B	TF binding region
ENSG00000237837	TF binding region
IGKV2OR2-10	TF binding region
IGKV1OR2-9	TF binding region
ENSG00000235833	TF binding region
IGKV1OR2-6	TF binding region
ENSG00000241481	TF binding region
ENSG00000230606	TF binding region
IGKV2OR2-7D	TF binding region
ANKRD36	TF binding region
IGKV2OR2-7	TF binding region
IGKV2OR2-8	TF binding region
IGKV1OR2-11	TF binding region
IGKV3OR2-5	TF binding region
ENSG00000271569	chromatin interactions
ENSG00000201806	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000228486	chromatin interactions
ENSG00000270252	chromatin interactions
C12orf29	miRNA target sites
EIF4G3	miRNA target sites
LYSMD1	miRNA target sites

Extended variants
information (count: 5277 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:5277 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4300875	chr2:97859833-97859834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554672951	chr2:97859878-97859879	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148820204	chr2:97859904-97859905	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540806496	chr2:97859911-97859912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143461484	chr2:97859954-97859955	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199866563	chr2:97859963-97859964	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546407955	chr2:97859990-97859991	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577120218	chr2:97859996-97859997	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546131850	chr2:97860016-97860017	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4092199	chr2:97860043-97860044	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs185179842	chr2:97860064-97860065	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541922225	chr2:97860078-97860079	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189684044	chr2:97860123-97860124	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527808225	chr2:97860126-97860127	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143747853	chr2:97860150-97860151	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113664043	chr2:97860180-97860181	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566713683	chr2:97860184-97860185	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532405846	chr2:97860185-97860186	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552502314	chr2:97860222-97860223	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4530406	chr2:97860223-97860224	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs200079700	chr2:97860234-97860235	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77475041	chr2:97860247-97860248	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77005786	chr2:97860248-97860249	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78510628	chr2:97860266-97860267	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11689120	chr2:97860276-97860277	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78288519	chr2:97860286-97860287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191854229	chr2:97860289-97860290	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77617259	chr2:97860301-97860302	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533699451	chr2:97860308-97860309	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79236556	chr2:97860311-97860312	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11677673	chr2:97860320-97860321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553939290	chr2:97860325-97860326	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77953976	chr2:97860332-97860333	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138832253	chr2:97860352-97860353	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546043390	chr2:97860353-97860354	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556452471	chr2:97860354-97860355	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199905832	chr2:97860355-97860356	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141284612	chr2:97860364-97860365	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561985448	chr2:97860376-97860377	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150846613	chr2:97860471-97860472	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs59466168	chr2:97860487-97860488	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541546995	chr2:97860488-97860489	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149975528	chr2:97860529-97860530	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560341527	chr2:97860536-97860537	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532368075	chr2:97860575-97860576	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200852589	chr2:97860581-97860582	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562787316	chr2:97860586-97860587	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370512076	chr2:97860602-97860603	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373728461	chr2:97860603-97860604	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548165599	chr2:97860611-97860612	Weak transcription Strong transcription Genic enhancers Enhancers	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97779800-97860400	Weak transcription	HMEC	breast
2	chr2:97779800-97877200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr2:97780000-97884600	Weak transcription	Fetal Stomach	stomach
4	chr2:97781000-97861800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:97808000-97867400	Weak transcription	Fetal Kidney	kidney
6	chr2:97811600-97862000	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:97816200-97881400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr2:97828600-97863200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr2:97833400-97882800	Weak transcription	Psoas Muscle	Psoas
10	chr2:97834600-97883000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:97835000-97861800	Weak transcription	Fetal Heart	heart
12	chr2:97835200-97866200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:97836000-97866400	Weak transcription	Primary B cells from cord blood	blood
14	chr2:97841200-97862800	Weak transcription	HepG2	liver
15	chr2:97841800-97867200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:97844400-97863200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr2:97844600-97879400	Weak transcription	Brain Germinal Matrix	brain
18	chr2:97844800-97860600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr2:97845800-97863200	Weak transcription	Colonic Mucosa	Colon
20	chr2:97846000-97889600	Weak transcription	NHLF	lung
21	chr2:97847200-97860000	Weak transcription	Left Ventricle	heart
22	chr2:97847200-97883000	Weak transcription	Placenta	Placenta
23	chr2:97847600-97865400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:97847800-97860600	Weak transcription	GM12878-XiMat	blood
25	chr2:97847800-97865600	Weak transcription	Pancreas	Pancrea
26	chr2:97848000-97865600	Weak transcription	Aorta	Aorta
27	chr2:97848000-97884800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr2:97848000-97884800	Weak transcription	Right Ventricle	heart
29	chr2:97848000-97886200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr2:97848400-97863200	Weak transcription	Hela-S3	cervix
31	chr2:97849200-97860600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:97849200-97865600	Weak transcription	NHEK	skin
33	chr2:97849600-97877200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:97849800-97879000	Weak transcription	Fetal Intestine Small	intestine
35	chr2:97850000-97863600	Weak transcription	Thymus	Thymus
36	chr2:97850200-97898800	Weak transcription	Small Intestine	intestine
37	chr2:97850800-97861800	Weak transcription	Brain Substantia Nigra	brain
38	chr2:97851000-97862000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr2:97851000-97863200	Weak transcription	A549	lung
40	chr2:97852600-97862400	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr2:97853600-97876200	Weak transcription	Lung	lung
42	chr2:97855000-97868600	Strong transcription	Fetal Thymus	thymus
43	chr2:97855400-97869400	Weak transcription	Gastric	stomach
44	chr2:97855600-97871400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr2:97855600-97897000	Weak transcription	Spleen	Spleen
46	chr2:97856000-97871200	Weak transcription	HSMMtube	muscle
47	chr2:97856200-97860600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:97856200-97861400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:97856200-97864200	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr2:97856200-97864400	Strong transcription	HUES48 Cell Line	embryonic stem cell

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