Variant report

Variant	esv19987
Chromosome Location	chr2:98856422-98886491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:98885630-98885941	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:98877882-98877971	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:98885740-98885741	K562	blood:	n/a	n/a
4	CBX3	chr2:98884799-98885003	K562	blood:	n/a	n/a
5	CBX3	chr2:98879878-98880163	K562	blood:	n/a	n/a
6	CEBPB	chr2:98885647-98886154	H1-hESC	embryonic stem cell:	n/a	chr2:98886062-98886073
7	CEBPB	chr2:98885701-98886249	Hela-S3	cervix:	n/a	chr2:98886062-98886073
8	CEBPB	chr2:98885559-98886413	HCT-116	colon:	n/a	chr2:98886062-98886073
9	CEBPB	chr2:98885881-98886204	K562	blood:	n/a	chr2:98886062-98886073
10	CEBPB	chr2:98885844-98886176	A549	lung:	n/a	chr2:98886062-98886073
11	CEBPB	chr2:98885784-98886245	IMR90	lung:	n/a	chr2:98886062-98886073
12	CEBPB	chr2:98885557-98886337	HCT-116	colon:	n/a	chr2:98886062-98886073
13	CEBPB	chr2:98885814-98886114	K562	blood:	n/a	chr2:98886062-98886073
14	CEBPB	chr2:98885807-98886190	HepG2	liver:	n/a	chr2:98886062-98886073
15	CHD2	chr2:98885738-98886118	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr2:98885631-98886043	GM12878	blood:	n/a	n/a
17	CTCF	chr2:98885740-98885890	AG09309	skin:	n/a	n/a
18	CTCF	chr2:98885740-98885890	A549	lung:	n/a	n/a
19	CTCF	chr2:98885760-98885910	Caco-2	colon:	n/a	n/a
20	CTCF	chr2:98885686-98885918	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr2:98885589-98886096	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:98885780-98885930	BE2_C	brain:	n/a	n/a
23	CTCF	chr2:98886020-98886170	NHEK	skin:	n/a	n/a
24	CTCF	chr2:98885678-98885957	ECC-1	luminal epithelium:	n/a	n/a
25	CTCF	chr2:98885780-98885930	HAc	cerebellar:	n/a	n/a
26	CTCF	chr2:98885712-98885960	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr2:98885740-98885890	HFF	foreskin:	n/a	n/a
28	CTCF	chr2:98885732-98885942	K562	blood:	n/a	n/a
29	CTCF	chr2:98885731-98885928	Medullo	brain:	n/a	n/a
30	CTCF	chr2:98885780-98885930	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr2:98885600-98885750	HAc	cerebellar:	n/a	n/a
32	CTCF	chr2:98885780-98885930	GM12872	blood:	n/a	n/a
33	CTCF	chr2:98885704-98885977	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr2:98885760-98885910	HEK293	kidney:	n/a	n/a
35	CTCF	chr2:98886240-98886390	AG10803	skin:	n/a	n/a
36	CTCF	chr2:98885760-98885910	AG04450	lung:	n/a	n/a
37	CTCF	chr2:98885704-98885977	GM12878	blood:	n/a	n/a
38	CTCF	chr2:98885980-98886130	GM12868	blood:	n/a	n/a
39	CTCF	chr2:98885702-98885973	Gliobla	brain:	n/a	n/a
40	CTCF	chr2:98885740-98885890	BJ	skin:	n/a	n/a
41	CTCF	chr2:98885740-98885890	HRE	kidney:	n/a	n/a
42	CTCF	chr2:98885636-98886009	K562	blood:	n/a	n/a
43	CTCF	chr2:98885760-98885910	BE2_C	brain:	n/a	n/a
44	CTCF	chr2:98885708-98885965	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr2:98885603-98885948	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:98885960-98886110	A549	lung:	n/a	n/a
47	CTCF	chr2:98885740-98885890	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr2:98885712-98885964	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr2:98885760-98885910	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr2:98885740-98885890	HFF-Myc	foreskin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98885650-98885700	AG09309	skin:	n/a
2	chr2:98858136-98858186	HNPCEpiC	eye:	n/a
3	chr2:98858011-98858061	K562	blood:	n/a
4	chr2:98858011-98858061	RPTEC	kidney:	n/a
5	chr2:98858136-98858186	SKMC	muscle:	n/a
6	chr2:98866217-98866267	H1-hESC	embryonic stem cell:	embryo
7	chr2:98858136-98858186	MCF-7	breast:	n/a
8	chr2:98858571-98858621	HRCEpiC	kidney:	n/a
9	chr2:98858136-98858186	BE2_C	brain:	n/a
10	chr2:98885650-98885700	ECC-1	luminal epithelium:	n/a
11	chr2:98858595-98858645	HCT-116	colon:	n/a
12	chr2:98885650-98885700	A549	lung:	n/a
13	chr2:98858136-98858186	HCM	heart:	n/a
14	chr2:98858011-98858061	Jurkat	blood:	n/a
15	chr2:98858595-98858645	PANC-1	pancreas:	n/a
16	chr2:98885650-98885700	RPTEC	kidney:	n/a
17	chr2:98885650-98885700	HUVEC	blood vessel:	n/a
18	chr2:98858011-98858061	NH-A	brain:	n/a
19	chr2:98865917-98865967	MCF10A-Er-Src	breast:	n/a
20	chr2:98858595-98858645	BE2_C	brain:	n/a
21	chr2:98858571-98858621	LNCaP	prostate:	n/a
22	chr2:98885650-98885700	BE2_C	brain:	n/a
23	chr2:98858011-98858061	T-47D	breast:	n/a
24	chr2:98885650-98885700	HRPEpiC	eye:	n/a
25	chr2:98858011-98858061	NT2-D1	testis:	n/a
26	chr2:98866217-98866267	HIPEpiC	eye:	n/a
27	chr2:98885650-98885700	K562	blood:	n/a
28	chr2:98858011-98858061	AG09309	skin:	n/a
29	chr2:98858571-98858621	BE2_C	brain:	n/a
30	chr2:98858571-98858621	HMEC	breast:	n/a
31	chr2:98858011-98858061	SKMC	muscle:	n/a
32	chr2:98858011-98858061	HMEC	breast:	n/a
33	chr2:98885650-98885700	CMK	blood:	n/a
34	chr2:98866217-98866267	T-47D	breast:	n/a
35	chr2:98885650-98885700	GM06990	blood:	n/a
36	chr2:98858595-98858645	GM12892	blood:	n/a
37	chr2:98865917-98865967	HepG2	liver:	n/a
38	chr2:98858011-98858061	SK-N-SH_RA	brain:	n/a
39	chr2:98885650-98885700	PANC-1	pancreas:	n/a
40	chr2:98866217-98866267	PrEC	prostate:	n/a
41	chr2:98866217-98866267	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:98866217-98866267	AG09319	gingival:	n/a
43	chr2:98865917-98865967	HCT-116	colon:	n/a
44	chr2:98865917-98865967	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:98858011-98858061	BE2_C	brain:	n/a
46	chr2:98858571-98858621	H1-hESC	embryonic stem cell:	embryo
47	chr2:98866217-98866267	HRE	kidney:	n/a
48	chr2:98858136-98858186	AG10803	skin:	n/a
49	chr2:98858595-98858645	HAEpiC	amniotic membrane:	n/a
50	chr2:98858595-98858645	BJ	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:98868004..98870745-chr2:98873730..98876518,2	K562	blood:
2	chr2:98422785..98423811-chr2:98885571..98886436,3	MCF-7	breast:
3	chr2:98868004..98870745-chr2:98873730..98876518,2	K562	blood:
4	chr2:98849964..98853776-chr2:98854233..98857105,4	MCF-7	breast:
5	chr2:98326087..98326680-chr2:98885400..98886287,2	MCF-7	breast:
6	chr2:98611818..98613602-chr2:98884042..98885781,2	MCF-7	breast:
7	chr2:98316350..98317297-chr2:98885417..98886570,3	MCF-7	breast:
8	chr2:98611658..98614514-chr2:98866353..98868181,2	K562	blood:
9	chr2:98885600..98886159-chr2:99001199..99001715,2	MCF-7	breast:
10	chr2:98424321..98425194-chr2:98885366..98886224,2	K562	blood:

No data

Variant related genes	Relation type
VWA3B	TF binding region
VWA3B	CpG island
ENSG00000168658	chromatin interactions
ENSG00000075568	chromatin interactions

Extended variants
information (count: 650 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558450450	chr2:98856555-98856556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575065019	chr2:98856556-98856557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376262074	chr2:98856690-98856691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544016503	chr2:98856691-98856692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150282857	chr2:98856784-98856785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189871525	chr2:98856785-98856786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570129763	chr2:98856792-98856793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539998431	chr2:98856822-98856823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560084233	chr2:98856823-98856824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532044605	chr2:98856839-98856840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138888029	chr2:98856852-98856853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149406746	chr2:98856869-98856870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10170356	chr2:98856881-98856882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548811306	chr2:98856938-98856939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568416639	chr2:98856941-98856942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs62156686	chr2:98856960-98856961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11891512	chr2:98857001-98857002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570812023	chr2:98857048-98857049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539466927	chr2:98857055-98857056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs6731804	chr2:98857060-98857061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116439733	chr2:98857089-98857090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145823669	chr2:98857132-98857133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138746711	chr2:98857185-98857186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574586153	chr2:98857207-98857208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540307611	chr2:98857239-98857240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532282125	chr2:98857261-98857262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560018630	chr2:98857280-98857281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550450244	chr2:98857377-98857378	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs142680474	chr2:98857385-98857386	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563136230	chr2:98857445-98857446	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371697331	chr2:98857464-98857465	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs553054744	chr2:98857466-98857467	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532048571	chr2:98857469-98857470	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs4455212	chr2:98857601-98857602	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs568632938	chr2:98857605-98857606	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs138033148	chr2:98857619-98857620	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181628296	chr2:98857623-98857624	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547837660	chr2:98857637-98857638	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537722564	chr2:98857712-98857713	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs72950941	chr2:98857770-98857771	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs557004632	chr2:98857822-98857823	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs62156687	chr2:98857886-98857887	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs4535095	chr2:98857893-98857894	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs36102785	chr2:98857976-98857977	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537738847	chr2:98857979-98857980	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs554600720	chr2:98857987-98857988	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs574553021	chr2:98858102-98858103	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560772994	chr2:98858122-98858123	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76868564	chr2:98858136-98858137	Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs553405586	chr2:98858137-98858138	Enhancers Flanking Active TSS	TF binding region CpG island	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
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98851000-98857600	Weak transcription	Brain Substantia Nigra	brain
2	chr2:98851400-98856800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:98851600-98856800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:98854200-98857400	Weak transcription	Placenta	Placenta
5	chr2:98854400-98857400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:98855600-98857800	Weak transcription	Fetal Brain Male	brain
7	chr2:98856800-98858000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:98856800-98859200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr2:98857400-98857800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr2:98857400-98857800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr2:98857400-98857800	Enhancers	Placenta	Placenta
12	chr2:98857400-98858000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:98857400-98858000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:98857400-98858000	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:98857400-98858200	Enhancers	Brain Anterior Caudate	brain
16	chr2:98857400-98858200	Enhancers	Brain Hippocampus Middle	brain
17	chr2:98857400-98858400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr2:98857400-98859400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:98857400-98859400	Enhancers	Brain Germinal Matrix	brain
20	chr2:98857400-98859600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:98857600-98858000	Enhancers	Brain Angular Gyrus	brain
22	chr2:98857600-98858000	Enhancers	Brain Substantia Nigra	brain
23	chr2:98857600-98858600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:98857600-98859200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:98857800-98858200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
26	chr2:98857800-98858800	Enhancers	Fetal Brain Male	brain
27	chr2:98858000-98858200	Flanking Active TSS	Brain Angular Gyrus	brain
28	chr2:98858000-98858200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:98858000-98858400	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr2:98858000-98858400	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr2:98858000-98858800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:98858200-98858400	Enhancers	Brain Angular Gyrus	brain
33	chr2:98858200-98858400	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr2:98858200-98858400	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr2:98858200-98858400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:98858200-98858800	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr2:98858400-98858800	Active TSS	Brain Anterior Caudate	brain
38	chr2:98858400-98858800	Active TSS	Brain Cingulate Gyrus	brain
39	chr2:98858400-98858800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr2:98858400-98859000	Active TSS	Brain Angular Gyrus	brain
41	chr2:98858400-98859000	Active TSS	Brain Hippocampus Middle	brain
42	chr2:98858400-98859000	Active TSS	Brain Substantia Nigra	brain
43	chr2:98858800-98859200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:98858800-98859200	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr2:98858800-98859200	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr2:98858800-98859200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr2:98858800-98859200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:98859000-98859200	Flanking Active TSS	Brain Angular Gyrus	brain
49	chr2:98859000-98859200	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr2:98859000-98859200	Flanking Active TSS	Brain Substantia Nigra	brain

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