Variant report

Variant	nsv1006679
Chromosome Location	chr2:97886322-98162177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1145)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:158)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr2:97913986-97914232	GM12878	blood:	n/a	n/a
3	BATF	chr2:98096813-98097157	GM12878	blood:	n/a	n/a
4	BATF	chr2:98096792-98097131	GM12878	blood:	n/a	n/a
5	BATF	chr2:97942129-97942430	GM12878	blood:	n/a	n/a
6	BATF	chr2:98158810-98158993	GM12878	blood:	n/a	n/a
7	BATF	chr2:98137602-98137837	GM12878	blood:	n/a	n/a
8	BATF	chr2:97901525-97901760	GM12878	blood:	n/a	n/a
9	BATF	chr2:97942120-97942451	GM12878	blood:	n/a	n/a
10	BATF	chr2:98139756-98139918	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:98139694-98139945	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:97899417-97899668	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:97906395-97906622	HepG2	liver:	n/a	n/a
14	BHLHE40	chr2:98132740-98132967	HepG2	liver:	n/a	n/a
15	CBX3	chr2:97896489-97896815	K562	blood:	n/a	n/a
16	CEBPB	chr2:98019815-98020123	A549	lung:	n/a	chr2:98019886-98019897
17	CEBPB	chr2:98018225-98018551	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:98018246-98018416	A549	lung:	n/a	n/a
19	CHD2	chr2:98025044-98025343	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr2:98067977-98068088	HepG2	liver:	n/a	chr2:98068023-98068041
21	CTCF	chr2:97970774-97970948	Spleen_OC	spleen:	n/a	chr2:97970855-97970873
22	CTCF	chr2:98105392-98105473	GM10248	blood:	n/a	n/a
23	CTCF	chr2:98158391-98158472	GM13976	blood:	n/a	n/a
24	CTCF	chr2:98017560-98017718	GM12878	blood:	n/a	n/a
25	CTCF	chr2:97970721-97970930	MCF-7	breast:	n/a	chr2:97970855-97970873
26	CTCF	chr2:98017572-98017698	GM19240	blood:	n/a	n/a
27	CTCF	chr2:98017560-98017710	GM12875	blood:	n/a	n/a
28	CTCF	chr2:98148381-98148515	GM13976	blood:	n/a	n/a
29	CTCF	chr2:98017520-98017670	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr2:98017555-98017649	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr2:98066369-98066445	LNCaP	prostate:	n/a	n/a
32	CTCF	chr2:97976092-97976343	A549	lung:	n/a	n/a
33	CTCF	chr2:97993467-97993519	GM20000	blood:	n/a	n/a
34	CTCF	chr2:98149997-98150060	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr2:97977096-97977138	LNCaP	prostate:	n/a	n/a
36	CTCF	chr2:98067926-98068122	HUVEC	blood vessel:	n/a	chr2:98068023-98068041
37	CTCF	chr2:98115849-98115882	Medullo	brain:	n/a	n/a
38	CTCF	chr2:98118020-98118072	Medullo	brain:	n/a	n/a
39	CTCF	chr2:98017526-98017738	GM12891	blood:	n/a	n/a
40	CTCF	chr2:97993468-97993593	LNCaP	prostate:	n/a	n/a
41	CTCF	chr2:97931207-97931215	GM20000	blood:	n/a	n/a
42	CTCF	chr2:97994077-97994139	GM13977	blood:	n/a	n/a
43	CTCF	chr2:98017516-98017762	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:97971374-97971383	A549	lung:	n/a	n/a
45	CTCF	chr2:98017580-98017730	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:98017500-98017650	AG04449	skin:	n/a	n/a
47	CTCF	chr2:98087828-98087837	GM13976	blood:	n/a	n/a
48	CTCF	chr2:98017546-98017729	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr2:97970770-97970960	LNCaP	prostate:	n/a	chr2:97970855-97970873
50	CTCF	chr2:97970728-97970931	GM12891	blood:	n/a	chr2:97970855-97970873

No data

(count:8 , 50 per page) page: 1

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

(count:158 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-1	chr2:97949672-97949910	NONHSAT072620
2	lnc-ACTR1B-4	chr2:98069548-98069799	XLOC_002217
3	lnc-ACTR1B-3	chr2:98088519-98088677	NONHSAT072644
4	lnc-ANKRD36-1	chr2:97957294-97957632	NONHSAT072616
5	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606
6	lnc-ACTR1B-3	chr2:98088770-98091049	ENSG00000230606
7	lnc-FAHD2B-4	chr2:97987331-97987617	NONHSAT072621
8	lnc-ACTR1B-3	chr2:98088032-98088090	ENSG00000230606.6
9	lnc-ACTR1B-3	chr2:98089391-98089662	ENSG00000230606.6
10	lnc-FAHD2B-1	chr2:97934421-97934440	XLOC_002214
11	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606.6
12	lnc-ACTR1B-9	chr2:98024520-98024800	NONHSAT072625
13	lnc-ACTR1B-8	chr2:98123499-98123528	NONHSAT072651
14	lnc-ACTR1B-3	chr2:98081774-98082014	ENSG00000230606.6
15	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072642
16	lnc-ACTR1B-3	chr2:98088173-98088252	NONHSAT072636
17	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
18	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072636
19	lnc-ANKRD36-1	chr2:97948299-97950522	XLOC_001583
20	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072638
21	lnc-ANKRD36-2	chr2:98086678-98086841	XLOC_001584
22	lnc-ACTR1B-3	chr2:98091457-98091651	ENSG00000230606.6
23	lnc-ACTR1B-3	chr2:98088032-98088090	NONHSAT072636
24	lnc-ACTR1B-3	chr2:98088173-98088252	ENSG00000230606.6
25	lnc-ACTR1B-3	chr2:98088576-98088677	ENSG00000230606.6
26	lnc-ACTR1B-1	chr2:98104748-98105157	XLOC_002220
27	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606
28	lnc-ACTR1B-3	chr2:98091457-98091693	ENSG00000230606.6
29	lnc-ACTR1B-3	chr2:98087567-98088252	NONHSAT072642
30	lnc-ACTR1B-3	chr2:98081812-98082014	ENSG00000230606.6
31	lnc-ACTR1B-3	chr2:98088770-98088854	ENSG00000230606.6
32	lnc-ACTR1B-3	chr2:98088173-98088252	ENSG00000230606.6
33	lnc-ACTR1B-3	chr2:98088032-98088252	ENSG00000230606.6
34	lnc-ACTR1B-3	chr2:98088548-98088677	ENSG00000230606.6
35	lnc-ACTR1B-8	chr2:98124458-98124528	NONHSAT072651
36	lnc-ACTR1B-3	chr2:98088032-98088249	ENSG00000230606.6
37	lnc-ANKRD36-1	chr2:97951040-97951260	NONHSAT072617
38	lnc-FAHD2B-2	chr2:97932879-97933133	XLOC_002216
39	lnc-ACTR1B-3	chr2:98088770-98088854	ENSG00000230606.6
40	lnc-ACTR1B-3	chr2:98089395-98089511	ENSG00000230606.6
41	lnc-ANKRD36-1	chr2:97950427-97950522	NONHSAT072620
42	lnc-ACTR1B-3	chr2:98087740-98088252	ENSG00000230606.6
43	lnc-ACTR1B-3	chr2:98088770-98091049	NR_040097
44	lnc-ANKRD36-1	chr2:97957294-97957632	NONHSAT072617
45	lnc-FAHD2B-1	chr2:97930723-97931774	XLOC_002214
46	lnc-ACTR1B-3	chr2:98088652-98088677	ENSG00000230606
47	lnc-ACTR1B-3	chr2:98088548-98088677	NONHSAT072631
48	lnc-ACTR1B-3	chr2:98088770-98088865	ENSG00000230606.6
49	lnc-ACTR1B-3	chr2:98088770-98090673	NONHSAT072638
50	lnc-ACTR1B-3	chr2:98089391-98089496	ENSG00000230606.6

No data

Variant related genes	Relation type
ANKRD36B	TF binding region
ENSG00000237837	TF binding region
ENSG00000235833	TF binding region
ANKRD36	TF binding region
IGKV2OR2-7	TF binding region
IGKV1OR2-11	TF binding region
IGKV3OR2-5	TF binding region
IGKV2OR2-10	TF binding region
IGKV1OR2-9	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
ENSG00000270252	chromatin interactions
ENSG00000271569	chromatin interactions
C12orf29	miRNA target sites
EIF4G3	miRNA target sites
LYSMD1	miRNA target sites

Extended variants
information (count: 2275 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2275 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566424597	chr2:97886323-97886324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377766063	chr2:97886330-97886331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568936472	chr2:97886371-97886372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537682840	chr2:97886394-97886395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186257204	chr2:97886428-97886429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141822456	chr2:97886467-97886468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61638245	chr2:97886484-97886485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367636938	chr2:97886485-97886486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142367295	chr2:97886496-97886497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200929945	chr2:97886498-97886499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139707918	chr2:97886499-97886500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60699692	chr2:97886508-97886509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57508674	chr2:97886510-97886511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28842495	chr2:97886511-97886512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28882240	chr2:97886513-97886514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28876511	chr2:97886526-97886527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58512786	chr2:97886527-97886528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568059086	chr2:97886577-97886578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184169164	chr2:97886610-97886611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28874632	chr2:97886671-97886672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576840420	chr2:97886674-97886675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59598686	chr2:97886690-97886691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59323388	chr2:97886699-97886700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376642685	chr2:97886722-97886723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370819276	chr2:97886761-97886762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60073322	chr2:97886797-97886798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566523391	chr2:97886805-97886806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs62156181	chr2:97886842-97886843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28839187	chr2:97886879-97886880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113966832	chr2:97887147-97887148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200438249	chr2:97887342-97887343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374083536	chr2:97887390-97887391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367935232	chr2:97887428-97887429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370284936	chr2:97887439-97887440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141178626	chr2:97887477-97887478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202158980	chr2:97887510-97887511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556253832	chr2:97887632-97887633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140042592	chr2:97887683-97887684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576547257	chr2:97887690-97887691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542483384	chr2:97887810-97887811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201714107	chr2:97887814-97887815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562366308	chr2:97887825-97887826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572780805	chr2:97887835-97887836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541395991	chr2:97887850-97887851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538855156	chr2:97887880-97887881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147008427	chr2:97887896-97887897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543535284	chr2:97887915-97887916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4645037	chr2:97887987-97887988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531398023	chr2:97887996-97887997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547982881	chr2:97888007-97888008	Weak transcription ZNF genes & repeats	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:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97846000-97889600	Weak transcription	NHLF	lung
2	chr2:97850200-97898800	Weak transcription	Small Intestine	intestine
3	chr2:97855600-97897000	Weak transcription	Spleen	Spleen
4	chr2:97863800-97891600	Weak transcription	Liver	Liver
5	chr2:97863800-97896800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:97863800-97899000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:97864000-97893400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:97864000-97911600	Weak transcription	Colonic Mucosa	Colon
9	chr2:97864200-97899000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr2:97866600-97888200	Weak transcription	Pancreas	Pancrea
11	chr2:97866800-97902200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:97867200-97902200	Weak transcription	Brain Substantia Nigra	brain
13	chr2:97868000-97889800	Weak transcription	HSMM	muscle
14	chr2:97868600-97902000	Weak transcription	Colon Smooth Muscle	Colon
15	chr2:97868800-97886400	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr2:97868800-97897000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr2:97869000-97889600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr2:97869200-97896800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr2:97871800-97900800	Weak transcription	A549	lung
20	chr2:97875200-97886400	Weak transcription	Fetal Heart	heart
21	chr2:97876000-97887200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr2:97877600-97886400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:97877600-97890600	Weak transcription	HMEC	breast
24	chr2:97877600-97896400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:97877600-97896800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:97877600-97896800	Weak transcription	Brain Anterior Caudate	brain
27	chr2:97877600-97896800	Weak transcription	Thymus	Thymus
28	chr2:97877800-97887200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr2:97877800-97897000	Weak transcription	Fetal Muscle Leg	muscle
30	chr2:97877800-97898800	Weak transcription	Left Ventricle	heart
31	chr2:97878000-97892200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr2:97878000-97892600	Weak transcription	Hela-S3	cervix
33	chr2:97878000-97895400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr2:97878000-97896800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:97878000-97896800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr2:97878000-97896800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr2:97878000-97897000	Weak transcription	Fetal Intestine Large	intestine
38	chr2:97878000-97897800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr2:97878000-97898400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:97878000-97898400	Weak transcription	HUVEC	blood vessel
41	chr2:97878000-97899000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr2:97878000-97901000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr2:97878000-97902000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr2:97878000-97911400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr2:97878200-97887200	Weak transcription	Brain Angular Gyrus	brain
46	chr2:97878200-97893800	Weak transcription	Fetal Thymus	thymus
47	chr2:97878200-97896000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr2:97878200-97896800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:97878200-97896800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr2:97878200-97898600	Weak transcription	Muscle Satellite Cultured Cells	--

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