Variant report

Variant	nsv1008339
Chromosome Location	chr2:98013814-98162177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:629)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:125)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:98158810-98158993	GM12878	blood:	n/a	n/a
2	BATF	chr2:98137602-98137837	GM12878	blood:	n/a	n/a
3	BATF	chr2:98096813-98097157	GM12878	blood:	n/a	n/a
4	BATF	chr2:98139756-98139918	GM12878	blood:	n/a	n/a
5	BATF	chr2:98096792-98097131	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:98132740-98132967	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:98139694-98139945	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:98018225-98018551	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:98019815-98020123	A549	lung:	n/a	chr2:98019886-98019897
10	CEBPB	chr2:98018246-98018416	A549	lung:	n/a	n/a
11	CHD2	chr2:98025044-98025343	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr2:98017540-98017690	BE2_C	brain:	n/a	n/a
13	CTCF	chr2:98017519-98017749	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:98068001-98068106	Fibrobl	skin:	n/a	chr2:98068023-98068041
15	CTCF	chr2:98159687-98159697	LNCaP	prostate:	n/a	n/a
16	CTCF	chr2:98158391-98158472	GM13976	blood:	n/a	n/a
17	CTCF	chr2:98017516-98017762	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:98017660-98017810	HCM	heart:	n/a	n/a
19	CTCF	chr2:98017480-98017630	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr2:98017580-98017730	Caco-2	colon:	n/a	n/a
21	CTCF	chr2:98068008-98068099	H1-hESC	embryonic stem cell:	n/a	chr2:98068023-98068041
22	CTCF	chr2:98070685-98070752	GM10266	blood:	n/a	n/a
23	CTCF	chr2:98017520-98017670	HMF	breast:	n/a	n/a
24	CTCF	chr2:98111843-98111868	Medullo	brain:	n/a	n/a
25	CTCF	chr2:98017460-98017610	GM12866	blood:	n/a	n/a
26	CTCF	chr2:98068003-98068109	ProgFib	skin:	n/a	chr2:98068023-98068041
27	CTCF	chr2:98017560-98017710	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr2:98068002-98068045	GM10248	blood:	n/a	chr2:98068023-98068041
29	CTCF	chr2:98118020-98118072	Medullo	brain:	n/a	n/a
30	CTCF	chr2:98067941-98068137	GM12878	blood:	n/a	chr2:98068023-98068041
31	CTCF	chr2:98017580-98017730	A549	lung:	n/a	n/a
32	CTCF	chr2:98155511-98155562	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr2:98017540-98017690	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr2:98068002-98068090	GM19240	blood:	n/a	chr2:98068023-98068041
35	CTCF	chr2:98062596-98062657	Medullo	brain:	n/a	n/a
36	CTCF	chr2:98017509-98017746	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:98062515-98062766	A549	lung:	n/a	n/a
38	CTCF	chr2:98067928-98068136	A549	lung:	n/a	chr2:98068023-98068041
39	CTCF	chr2:98137517-98137596	Medullo	brain:	n/a	n/a
40	CTCF	chr2:98017600-98017750	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr2:98066369-98066445	LNCaP	prostate:	n/a	n/a
42	CTCF	chr2:98017260-98017410	GM12870	blood:	n/a	n/a
43	CTCF	chr2:98067917-98068151	LNCaP	prostate:	n/a	chr2:98068023-98068041
44	CTCF	chr2:98068010-98068052	Medullo	brain:	n/a	chr2:98068023-98068041
45	CTCF	chr2:98017600-98017750	AG04450	lung:	n/a	n/a
46	CTCF	chr2:98067967-98068131	GM12891	blood:	n/a	chr2:98068023-98068041
47	CTCF	chr2:98017551-98017731	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr2:98073649-98073708	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:98017593-98017700	HepG2	liver:	n/a	n/a
50	CTCF	chr2:98150890-98150978	Medullo	brain:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:98013225..98016520-chr2:98024524..98026822,3	MCF-7	breast:
2	chr2:98012288..98014989-chr2:98016179..98017699,2	MCF-7	breast:
3	chr2:98021214..98022721-chr2:98024555..98026401,2	K562	blood:
4	chr2:98019789..98021903-chr2:98023774..98026481,2	MCF-7	breast:
5	chr2:98013205..98013710-chr2:98025264..98025790,2	MCF-7	breast:
6	chr2:98012288..98014989-chr2:98016179..98017699,2	MCF-7	breast:
7	chr2:98015115..98017129-chr2:98018538..98021537,2	K562	blood:

(count:125 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
2	lnc-ACTR1B-3	chr2:98088089-98088677	ENSG00000230606
3	lnc-ACTR1B-3	chr2:98088173-98088252	ENSG00000230606.6
4	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072636
5	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
6	lnc-ACTR1B-3	chr2:98088770-98088854	ENSG00000230606.6
7	lnc-ACTR1B-8	chr2:98127601-98127712	NONHSAT072651
8	lnc-ACTR1B-3	chr2:98081928-98082014	NONHSAT072638
9	lnc-ACTR1B-3	chr2:98088770-98091049	NR_040097
10	lnc-ACTR1B-3	chr2:98087567-98088252	NONHSAT072642
11	lnc-ACTR1B-3	chr2:98088770-98088865	NONHSAT072631
12	lnc-ACTR1B-3	chr2:98088770-98088849	ENSG00000230606
13	lnc-ANKRD36-2	chr2:98086678-98086841	XLOC_001584
14	lnc-ACTR1B-3	chr2:98098880-98099067	ENSG00000230606.6
15	lnc-ACTR1B-2	chr2:98104121-98104135	XLOC_002219
16	lnc-ACTR1B-3	chr2:98088770-98088854	ENSG00000230606.6
17	lnc-ACTR1B-1	chr2:98105261-98105300	XLOC_002220
18	lnc-ACTR1B-3	chr2:98089391-98089511	ENSG00000230606.6
19	lnc-ACTR1B-3	chr2:98088032-98088249	ENSG00000230606.6
20	lnc-ACTR1B-8	chr2:98124027-98124120	NONHSAT072651
21	lnc-ACTR1B-3	chr2:98088032-98088090	NONHSAT072636
22	lnc-ACTR1B-3	chr2:98088032-98088252	NR_040097
23	lnc-ANKRD36-2	chr2:98086771-98086841	ENSG00000241481.2
24	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072631
25	lnc-ACTR1B-3	chr2:98089391-98089662	ENSG00000230606.6
26	lnc-ACTR1B-3	chr2:98089888-98089998	ENSG00000230606.6
27	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606
28	lnc-ACTR1B-4	chr2:98071668-98071970	XLOC_002217
29	lnc-ACTR1B-3	chr2:98088519-98088677	NONHSAT072644
30	lnc-ACTR1B-3	chr2:98088576-98088677	ENSG00000230606.6
31	lnc-ACTR1B-3	chr2:98098880-98099107	ENSG00000230606.6
32	lnc-ACTR1B-3	chr2:98091457-98091784	ENSG00000230606.6
33	lnc-ANKRD36-11	chr2:98041867-98042166	NONHSAT072627
34	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
35	lnc-ACTR1B-3	chr2:98088770-98091348	NONHSAT072642
36	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606.6
37	lnc-ACTR1B-3	chr2:98094797-98095220	ENSG00000230606.6
38	lnc-ACTR1B-6	chr2:98140412-98141439	NONHSAT072652
39	lnc-ACTR1B-3	chr2:98081922-98082014	ENSG00000230606.6
40	lnc-ACTR1B-3	chr2:98081851-98082014	NONHSAT072636
41	lnc-ACTR1B-3	chr2:98088770-98088981	ENSG00000230606.6
42	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
43	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
44	lnc-ACTR1B-3	chr2:98091457-98091637	ENSG00000230606.6
45	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072638
46	lnc-ACTR1B-3	chr2:98081083-98082014	ENSG00000230606.6
47	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606.6
48	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
49	lnc-ACTR1B-4	chr2:98069548-98069799	XLOC_002217
50	lnc-ACTR1B-3	chr2:98089382-98089511	ENSG00000230606.6

No data

Variant related genes	Relation type
ANKRD36B	TF binding region
ENSG00000237837	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
IGKV2OR2-8	TF binding region
IGKV3OR2-5	TF binding region
ENSG00000270252	chromatin interactions
ENSG00000271569	chromatin interactions
LYSMD1	miRNA target sites

Extended variants
information (count: 1308 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1308 , 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	rs4264593	chr2:98013814-98013815	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555661347	chr2:98013830-98013831	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369866398	chr2:98013841-98013842	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565700274	chr2:98013859-98013860	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572387394	chr2:98013861-98013862	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187966297	chr2:98013960-98013961	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557449613	chr2:98014003-98014004	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577604486	chr2:98014008-98014009	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75130976	chr2:98014067-98014068	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557020457	chr2:98014071-98014072	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs193012992	chr2:98014079-98014080	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542827408	chr2:98014085-98014086	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559589670	chr2:98014086-98014087	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375033415	chr2:98014093-98014094	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4586674	chr2:98014115-98014116	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185196652	chr2:98014146-98014147	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189801778	chr2:98014258-98014259	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17842456	chr2:98014319-98014320	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138844216	chr2:98014336-98014337	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567760060	chr2:98014347-98014348	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559492288	chr2:98014369-98014370	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140610563	chr2:98014409-98014410	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs145737985	chr2:98014430-98014431	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565912589	chr2:98014474-98014475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534902528	chr2:98014544-98014545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372524778	chr2:98014555-98014556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs60226695	chr2:98014565-98014566	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs537057690	chr2:98014629-98014630	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138203559	chr2:98014632-98014633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573421387	chr2:98014669-98014670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542340593	chr2:98014674-98014675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538275172	chr2:98014681-98014682	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192793463	chr2:98014698-98014699	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545373609	chr2:98014760-98014761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142798200	chr2:98014768-98014769	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs34147706	chr2:98014769-98014770	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570517079	chr2:98014772-98014773	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531212481	chr2:98014773-98014774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530772100	chr2:98014785-98014786	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544611329	chr2:98014789-98014790	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556260063	chr2:98014793-98014794	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561198229	chr2:98014800-98014801	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183547867	chr2:98014837-98014838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547152600	chr2:98014848-98014849	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565874568	chr2:98014853-98014854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188282992	chr2:98014868-98014869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs17037402	chr2:98014883-98014884	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs180904169	chr2:98014884-98014885	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535764005	chr2:98014939-98014940	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571531502	chr2:98014940-98014941	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98013200-98014200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:98013200-98014200	Enhancers	Placenta	Placenta
3	chr2:98013200-98014400	Enhancers	Placenta Amnion	Placenta Amnion
4	chr2:98013800-98014000	Bivalent Enhancer	HSMMtube	muscle
5	chr2:98017000-98020400	Enhancers	Primary B cells from peripheral blood	blood
6	chr2:98017200-98020000	Enhancers	Primary B cells from cord blood	blood
7	chr2:98020000-98020200	Bivalent Enhancer	Aorta	Aorta
8	chr2:98020000-98020400	Bivalent Enhancer	Primary B cells from cord blood	blood
9	chr2:98023600-98023800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:98023600-98024600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:98023800-98024400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:98024400-98025000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:98024600-98025000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:98024600-98025400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:98024600-98025400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:98024800-98025400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:98024800-98025400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:98025000-98025200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr2:98025000-98025200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:98025000-98025400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr2:98025000-98025400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:98025000-98025400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr2:98025000-98025400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:98025000-98025600	Enhancers	Placenta	Placenta
25	chr2:98105600-98108000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:98105600-98108000	Weak transcription	Fetal Muscle Leg	muscle
27	chr2:98105600-98108400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr2:98106200-98111800	Weak transcription	Fetal Brain Female	brain
29	chr2:98106600-98107000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:98106600-98107000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:98106600-98107000	ZNF genes & repeats	Fetal Stomach	stomach
32	chr2:98106800-98107000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:98106800-98107000	Enhancers	Fetal Muscle Trunk	muscle
34	chr2:98106800-98107000	ZNF genes & repeats	Fetal Thymus	thymus
35	chr2:98107000-98110600	Weak transcription	Fetal Thymus	thymus
36	chr2:98107000-98112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:98139000-98142000	Weak transcription	Fetal Brain Female	brain
38	chr2:98139600-98142400	Weak transcription	Primary B cells from cord blood	blood
39	chr2:98140400-98141800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:98140400-98142000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr2:98140400-98142200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr2:98140600-98143800	Weak transcription	Primary T cells from cord blood	blood
43	chr2:98140800-98142400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:98140800-98142400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:98140800-98152800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr2:98140800-98187600	Weak transcription	Fetal Stomach	stomach
47	chr2:98141200-98144800	Weak transcription	Thymus	Thymus
48	chr2:98141800-98144200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:98141800-98161000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr2:98141800-98162800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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