Variant report

Variant	esv17805
Chromosome Location	chr3:195662762-195733839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1947)
CpG islands
(count:1957)
Chromatin interactive
region (count:16)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1947 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
3	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
4	ATF3	chr3:195717067-195717371	A549	lung:	n/a	n/a
5	ATF3	chr3:195678739-195678871	K562	blood:	n/a	n/a
6	ATF3	chr3:195717483-195717694	K562	blood:	n/a	n/a
7	ATF3	chr3:195717064-195717382	K562	blood:	n/a	n/a
8	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
9	ATF3	chr3:195717164-195717371	K562	blood:	n/a	n/a
10	BACH1	chr3:195717045-195717538	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
12	BATF	chr3:195717540-195717834	GM12878	blood:	n/a	n/a
13	BATF	chr3:195682771-195683491	GM12878	blood:	n/a	n/a
14	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
15	BATF	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
16	BATF	chr3:195682768-195683488	GM12878	blood:	n/a	n/a
17	BATF	chr3:195705475-195705667	GM12878	blood:	n/a	chr3:195705640-195705649 chr3:195705599-195705610
18	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
19	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
20	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
21	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
23	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
24	BCL11A	chr3:195662910-195663112	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:195681860-195682057	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:195682895-195683356	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:195682872-195683277	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
29	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
30	BCL11A	chr3:195711556-195711737	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
32	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
34	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
35	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
36	BCL11A	chr3:195722372-195722606	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:195723014-195723259	GM12878	blood:	n/a	chr3:195723080-195723089
38	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
39	BCL11A	chr3:195663537-195663765	GM12878	blood:	n/a	chr3:195663586-195663595
40	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
41	BCL3	chr3:195700608-195700811	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
43	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
44	BHLHE40	chr3:195717520-195717617	K562	blood:	n/a	n/a
45	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
46	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
47	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
48	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
49	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr3:195687930-195689486	K562	blood:	n/a	n/a

(count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195717574-195717624	BE2_C	brain:	n/a
2	chr3:195703920-195703970	MCF10A-Er-Src	breast:	n/a
3	chr3:195716626-195716676	Jurkat	blood:	n/a
4	chr3:195714100-195714150	Hepatocyte	liver:	n/a
5	chr3:195678176-195678226	HCM	heart:	n/a
6	chr3:195717574-195717624	BE2_C	brain:	n/a
7	chr3:195703920-195703970	MCF10A-Er-Src	breast:	n/a
8	chr3:195716626-195716676	Jurkat	blood:	n/a
9	chr3:195714100-195714150	Hepatocyte	liver:	n/a
10	chr3:195678176-195678226	HCM	heart:	n/a
11	chr3:195719790-195719840	SK-N-SH_RA	brain:	n/a
12	chr3:195717574-195717624	HCPEpiC	choroid plexus:	n/a
13	chr3:195679450-195679500	SK-N-MC	brain:	n/a
14	chr3:195681091-195681141	HEK293	kidney:	embryo
15	chr3:195709715-195709765	IMR90	lung:	fetal
16	chr3:195682595-195682645	HRE	kidney:	n/a
17	chr3:195668262-195668312	HCPEpiC	choroid plexus:	n/a
18	chr3:195714100-195714150	HUVEC	blood vessel:	n/a
19	chr3:195703920-195703970	HCF	heart:	n/a
20	chr3:195682595-195682645	CMK	blood:	n/a
21	chr3:195716626-195716676	Hela-S3	cervix:	n/a
22	chr3:195716626-195716676	SKMC	muscle:	n/a
23	chr3:195709661-195709711	Caco-2	colon:	n/a
24	chr3:195717344-195717394	PFSK-1	brain:	n/a
25	chr3:195668262-195668312	GM12892	blood:	n/a
26	chr3:195724371-195724421	AoSMC	blood vessel:	n/a
27	chr3:195679450-195679500	HMEC	breast:	n/a
28	chr3:195682326-195682376	BE2_C	brain:	n/a
29	chr3:195717416-195717466	AoSMC	blood vessel:	n/a
30	chr3:195717574-195717624	AG09309	skin:	n/a
31	chr3:195717344-195717394	SK-N-SH	brain:	n/a
32	chr3:195717574-195717624	AG04449	skin:	fetal
33	chr3:195700735-195700785	Hela-S3	cervix:	n/a
34	chr3:195719790-195719840	PFSK-1	brain:	n/a
35	chr3:195709698-195709748	NHBE	bronchial:	n/a
36	chr3:195701166-195701216	GM12891	blood:	n/a
37	chr3:195723614-195723664	Caco-2	colon:	n/a
38	chr3:195714100-195714150	ProgFib	skin:	n/a
39	chr3:195701166-195701216	GM12892	blood:	n/a
40	chr3:195683635-195683685	HRCEpiC	kidney:	n/a
41	chr3:195717344-195717394	HEK293	kidney:	embryo
42	chr3:195687741-195687791	HIPEpiC	eye:	n/a
43	chr3:195717344-195717394	BJ	skin:	n/a
44	chr3:195717344-195717394	AG09309	skin:	n/a
45	chr3:195709661-195709711	AG04449	skin:	fetal
46	chr3:195717962-195718012	PANC-1	pancreas:	n/a
47	chr3:195724371-195724421	BE2_C	brain:	n/a
48	chr3:195717344-195717394	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:195715851-195715901	HCM	heart:	n/a
50	chr3:195719790-195719840	BJ	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
2	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:
3	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
4	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:
5	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
6	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:
7	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
8	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
9	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:
10	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
11	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
12	chr3:195673861..195675995-chr5:278201..279705,3	K562	blood:
13	chr3:195655412..195657166-chr3:195660620..195663176,2	K562	blood:
14	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
15	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
16	chr3:195586120..195586802-chr3:195721315..195721912,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFRC-1	chr3:195666274-195667064	NONHSAT094272
2	lnc-TFRC-1	chr3:195726007-195726255	NONHSAT094273
3	lnc-TNK2-2	chr3:195665538-195665609	NONHSAT094271
4	lnc-TFRC-1	chr3:195726821-195726902	NONHSAT094273
5	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1
6	lnc-MUC20-9	chr3:195674996-195675559	NONHSAT094276
7	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275
8	lnc-TFRC-1	chr3:195666277-195666553	NONHSAT094273
9	lnc-TFRC-1	chr3:195668449-195672581	NONHSAT094272
10	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-
11	lnc-TNK2-2	chr3:195673684-195674350	NONHSAT094275
12	lnc-TNK2-2	chr3:195674206-195674576	NONHSAT094271

No data

Variant related genes	Relation type
ENSG00000231443	TF binding region
SDHAP1	TF binding region
ENSG00000231464	TF binding region
ENSG00000260261	TF binding region
ENSG00000231443	CpG island
SDHAP1	CpG island
ENSG00000231464	CpG island
ENSG00000260261	CpG island
ENSG00000242086	chromatin interactions
ENSG00000273009	chromatin interactions
ENSG00000215837	chromatin interactions
ENSG00000266730	chromatin interactions
ENSG00000229178	chromatin interactions
ENSG00000239122	chromatin interactions
ENSG00000061938	chromatin interactions

Extended variants
information (count: 3710 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3710 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72499654	chr3:195662770-195662771	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563162215	chr3:195662785-195662786	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530863726	chr3:195662793-195662794	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112906500	chr3:195662812-195662813	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2448529	chr3:195662858-195662859	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs140383223	chr3:195662866-195662867	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs6791829	chr3:195662887-195662888	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552462592	chr3:195662902-195662903	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs200155733	chr3:195662906-195662907	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs570852196	chr3:195662942-195662943	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531909661	chr3:195662946-195662947	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550177013	chr3:195662953-195662954	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376257412	chr3:195662961-195662962	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568348398	chr3:195662970-195662971	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535965549	chr3:195663006-195663007	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372774573	chr3:195663040-195663041	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566680628	chr3:195663063-195663064	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534016645	chr3:195663067-195663068	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558779724	chr3:195663087-195663088	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs56287907	chr3:195663117-195663118	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs577092317	chr3:195663133-195663134	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs185504732	chr3:195663170-195663171	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556142695	chr3:195663179-195663180	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574326668	chr3:195663182-195663183	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2638914	chr3:195663197-195663198	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559778388	chr3:195663230-195663231	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148379872	chr3:195663308-195663309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527377874	chr3:195663323-195663324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546036965	chr3:195663357-195663358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62284396	chr3:195663379-195663380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188032470	chr3:195663398-195663399	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs4927683	chr3:195663411-195663412	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs17092229	chr3:195663468-195663469	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
34	rs1688745	chr3:195663472-195663473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550178032	chr3:195663511-195663512	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs62284397	chr3:195663513-195663514	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs62284398	chr3:195663530-195663531	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201936458	chr3:195663537-195663538	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201111759	chr3:195663564-195663565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529230394	chr3:195663577-195663578	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs547802201	chr3:195663581-195663582	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566222327	chr3:195663615-195663616	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs62284399	chr3:195663649-195663650	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546705834	chr3:195663665-195663666	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs373843423	chr3:195663753-195663754	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs146885871	chr3:195663880-195663881	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs367763569	chr3:195663957-195663958	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs370328776	chr3:195664054-195664055	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558818477	chr3:195664074-195664075	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs367634073	chr3:195664075-195664076	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2082 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195666600	Weak transcription	Lung	lung
3	chr3:195648600-195666600	Weak transcription	Spleen	Spleen
4	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
5	chr3:195648800-195666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:195648800-195666800	Weak transcription	Esophagus	oesophagus
7	chr3:195651200-195671200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:195651800-195673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:195653000-195666800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:195656800-195666600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:195656800-195666600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr3:195656800-195669200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:195656800-195671200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:195657000-195666800	Weak transcription	Primary T cells from cord blood	blood
18	chr3:195657200-195666800	Weak transcription	Thymus	Thymus
19	chr3:195657400-195670000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
21	chr3:195658400-195666800	Weak transcription	Gastric	stomach
22	chr3:195658800-195666800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:195659000-195667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
25	chr3:195659600-195666600	Weak transcription	Brain Anterior Caudate	brain
26	chr3:195659600-195666800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
29	chr3:195660000-195666600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:195660000-195666600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:195660000-195666600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr3:195660000-195666600	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:195660000-195666800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:195660000-195666800	Weak transcription	Brain Substantia Nigra	brain
35	chr3:195660000-195666800	Weak transcription	Fetal Intestine Large	intestine
36	chr3:195660000-195666800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr3:195660000-195669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
39	chr3:195660200-195666600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:195660400-195666600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:195660400-195666800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:195660400-195666800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:195660600-195666400	Weak transcription	Fetal Intestine Small	intestine
45	chr3:195660600-195666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:195660600-195669600	Weak transcription	A549	lung
47	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr3:195660800-195666800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr3:195660800-195667000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:195660800-195669400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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