Variant report

Variant	esv1816915
Chromosome Location	chr7:99901968-99932858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:488)
Chromatin interactive
region (count:6)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:99932699-99932942	GM12878	blood:	n/a	n/a
2	BATF	chr7:99902780-99903057	GM12878	blood:	n/a	n/a
3	BATF	chr7:99902374-99902726	GM12878	blood:	n/a	n/a
4	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
5	BATF	chr7:99931291-99931464	GM12878	blood:	n/a	n/a
6	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
7	BATF	chr7:99931789-99932008	GM12878	blood:	n/a	n/a
8	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
9	BATF	chr7:99902062-99903018	GM12878	blood:	n/a	n/a
10	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
11	BATF	chr7:99922916-99923120	GM12878	blood:	n/a	n/a
12	BATF	chr7:99931763-99932072	GM12878	blood:	n/a	n/a
13	BATF	chr7:99902075-99902343	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
15	BCL11A	chr7:99902728-99903004	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:99902084-99902502	GM12878	blood:	n/a	chr7:99902302-99902311
17	BCL11A	chr7:99931290-99931519	GM12878	blood:	n/a	chr7:99931369-99931378
18	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:99931855-99932416	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:99902046-99902591	GM12878	blood:	n/a	chr7:99902302-99902311
22	BCL11A	chr7:99903987-99904347	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:99922824-99923053	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:99931741-99932177	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99929074-99929275	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
27	BCL11A	chr7:99922866-99923130	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
29	BCL11A	chr7:99931278-99931549	GM12878	blood:	n/a	chr7:99931369-99931378
30	BHLHE40	chr7:99918692-99918940	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:99926086-99926279	Hela-S3	cervix:	n/a	chr7:99926106-99926117
32	CEBPB	chr7:99926097-99926126	K562	blood:	n/a	chr7:99926106-99926117
33	CEBPB	chr7:99925950-99926249	K562	blood:	n/a	chr7:99926106-99926117
34	CEBPB	chr7:99926091-99926277	IMR90	lung:	n/a	chr7:99926106-99926117
35	CEBPB	chr7:99926090-99926280	HepG2	liver:	n/a	chr7:99926106-99926117
36	CHD1	chr7:99932051-99932082	GM12878	blood:	n/a	n/a
37	CTCF	chr7:99930547-99930585	GM10266	blood:	n/a	n/a
38	EBF1	chr7:99924565-99924827	GM12878	blood:	n/a	n/a
39	EBF1	chr7:99922035-99922479	GM12878	blood:	n/a	chr7:99922279-99922288 chr7:99922279-99922288 chr7:99922278-99922289 chr7:99922279-99922289
40	EBF1	chr7:99915877-99916141	GM12878	blood:	n/a	n/a
41	EBF1	chr7:99931769-99932106	GM12878	blood:	n/a	n/a
42	EBF1	chr7:99904888-99905056	GM12878	blood:	n/a	n/a
43	EBF1	chr7:99904117-99904433	GM12878	blood:	n/a	n/a
44	EBF1	chr7:99921189-99921874	GM12878	blood:	n/a	n/a
45	EBF1	chr7:99902013-99902505	GM12878	blood:	n/a	n/a
46	EBF1	chr7:99931284-99931455	GM12878	blood:	n/a	n/a
47	EBF1	chr7:99921178-99921996	GM12878	blood:	n/a	n/a
48	EBF1	chr7:99922050-99922565	GM12878	blood:	n/a	chr7:99922279-99922288 chr7:99922279-99922288 chr7:99922278-99922289 chr7:99922279-99922289
49	EBF1	chr7:99918743-99919003	GM12878	blood:	n/a	n/a
50	EBF1	chr7:99902022-99902661	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99904875-99904925	HEEpiC	esophagus:	n/a
2	chr7:99904850-99904900	U87	brain:	n/a
3	chr7:99904850-99904900	GM12878	blood:	n/a
4	chr7:99929438-99929488	AG10803	skin:	n/a
5	chr7:99912131-99912181	K562	blood:	n/a
6	chr7:99932089-99932139	HCPEpiC	choroid plexus:	n/a
7	chr7:99905334-99905384	HCT-116	colon:	n/a
8	chr7:99912131-99912181	HMEC	breast:	n/a
9	chr7:99932089-99932139	Hela-S3	cervix:	n/a
10	chr7:99904850-99904900	K562	blood:	n/a
11	chr7:99905334-99905384	NH-A	brain:	n/a
12	chr7:99918120-99918170	HIPEpiC	eye:	n/a
13	chr7:99918120-99918170	GM12878	blood:	n/a
14	chr7:99905334-99905384	AG10803	skin:	n/a
15	chr7:99904875-99904925	HAEpiC	amniotic membrane:	n/a
16	chr7:99904875-99904925	AG04450	lung:	fetal
17	chr7:99929438-99929488	H1-hESC	embryonic stem cell:	embryo
18	chr7:99929438-99929488	AG09319	gingival:	n/a
19	chr7:99905334-99905384	HRPEpiC	eye:	n/a
20	chr7:99904850-99904900	HRPEpiC	eye:	n/a
21	chr7:99905331-99905381	HUVEC	blood vessel:	n/a
22	chr7:99918120-99918170	GM12891	blood:	n/a
23	chr7:99905334-99905384	PrEC	prostate:	n/a
24	chr7:99912131-99912181	U87	brain:	n/a
25	chr7:99932089-99932139	K562	blood:	n/a
26	chr7:99932089-99932139	SK-N-SH	brain:	n/a
27	chr7:99904850-99904900	ECC-1	luminal epithelium:	n/a
28	chr7:99929438-99929488	NB4	blood:	n/a
29	chr7:99904875-99904925	HUVEC	blood vessel:	n/a
30	chr7:99918120-99918170	HEK293	kidney:	embryo
31	chr7:99918120-99918170	HCF	heart:	n/a
32	chr7:99905331-99905381	GM06990	blood:	n/a
33	chr7:99929438-99929488	SAEC	small airway:	n/a
34	chr7:99932089-99932139	ovcar-3	ovarian:	n/a
35	chr7:99912131-99912181	Hepatocyte	liver:	n/a
36	chr7:99905331-99905381	HRE	kidney:	n/a
37	chr7:99932089-99932139	SK-N-SH_RA	brain:	n/a
38	chr7:99932089-99932139	U87	brain:	n/a
39	chr7:99905331-99905381	SK-N-SH	brain:	n/a
40	chr7:99905334-99905384	SAEC	small airway:	n/a
41	chr7:99912131-99912181	HIPEpiC	eye:	n/a
42	chr7:99912131-99912181	HCF	heart:	n/a
43	chr7:99904850-99904900	HCPEpiC	choroid plexus:	n/a
44	chr7:99905331-99905381	CMK	blood:	n/a
45	chr7:99904850-99904900	GM12891	blood:	n/a
46	chr7:99905334-99905384	SK-N-SH	brain:	n/a
47	chr7:99904875-99904925	AG10803	skin:	n/a
48	chr7:99904850-99904900	NHBE	bronchial:	n/a
49	chr7:99905331-99905381	PFSK-1	brain:	n/a
50	chr7:99904850-99904900	GM12892	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99932349..99935076-chr7:100025979..100028387,3	K562	blood:
2	chr7:99715815..99718290-chr7:99932504..99934640,2	MCF-7	breast:
3	chr7:99932234..99937909-chr7:99939373..99942446,6	K562	blood:
4	chr7:99931911..99935442-chr7:99938364..99941933,5	MCF-7	breast:
5	chr7:99932595..99935080-chr7:100025979..100028387,3	K562	blood:
6	chr7:99932318..99935048-chr7:100026420..100028378,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GATS-3	chr7:99928086-99928176	NONHSAT122354
2	lnc-GATS-3	chr7:99927647-99927907	NONHSAT122354
3	lnc-GATS-2	chr7:99913916-99914300	expReg_chr7_6439_-
4	lnc-GATS-1	chr7:99907941-99908299	expReg_chr7_6426_-

No data

Variant related genes	Relation type
PMS2P1	TF binding region
STAG3L5P	TF binding region
PILRB	TF binding region
SPDYE3	TF binding region
STAG3L5P-PVRIG2P-PILRB	TF binding region
ENSG00000201913	TF binding region
PMS2P1	CpG island
STAG3L5P	CpG island
PILRB	CpG island
SPDYE3	CpG island
STAG3L5P-PVRIG2P-PILRB	CpG island
ENSG00000201913	CpG island
ENSG00000078319	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000106290	chromatin interactions

Extended variants
information (count: 933 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527786186	chr7:99901981-99901982	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs543077586	chr7:99901988-99901989	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561877555	chr7:99902019-99902020	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529081249	chr7:99902063-99902064	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550943695	chr7:99902073-99902074	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569166719	chr7:99902131-99902132	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs533215940	chr7:99902142-99902143	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551095867	chr7:99902192-99902193	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566436641	chr7:99902214-99902215	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs533667428	chr7:99902280-99902281	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555029646	chr7:99902287-99902288	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs193241312	chr7:99902298-99902299	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538045665	chr7:99902307-99902308	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556479151	chr7:99902343-99902344	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs578192853	chr7:99902363-99902364	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528828806	chr7:99902396-99902397	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs553899281	chr7:99902400-99902401	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs184077133	chr7:99902482-99902483	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112753786	chr7:99902593-99902594	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs201273240	chr7:99902638-99902639	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs561344184	chr7:99902643-99902644	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548230832	chr7:99902655-99902656	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547333503	chr7:99902759-99902760	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs62482195	chr7:99902890-99902891	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529144494	chr7:99902967-99902968	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544430124	chr7:99903027-99903028	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571237578	chr7:99903107-99903108	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs538644880	chr7:99903168-99903169	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs562628507	chr7:99903173-99903174	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs533100579	chr7:99903174-99903175	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs1137952	chr7:99903182-99903183	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs150352309	chr7:99903184-99903185	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs1137951	chr7:99903212-99903213	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138015869	chr7:99903238-99903239	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539016187	chr7:99903443-99903444	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs527259771	chr7:99903464-99903465	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs548716297	chr7:99903493-99903494	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567012128	chr7:99903531-99903532	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs199816282	chr7:99903570-99903571	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537505148	chr7:99903585-99903586	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs147212529	chr7:99903728-99903729	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542923711	chr7:99903733-99903734	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571783094	chr7:99903737-99903738	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538975895	chr7:99903757-99903758	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs554427832	chr7:99903758-99903759	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113017150	chr7:99903833-99903834	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs112619499	chr7:99903837-99903838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs554963562	chr7:99903844-99903845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576616169	chr7:99903867-99903868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543910234	chr7:99903877-99903878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99916800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:99870200-99932800	Weak transcription	Ovary	ovary
3	chr7:99870400-99904600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
8	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:99870600-99904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
12	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:99870800-99904600	Weak transcription	Dnd41	blood
15	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
17	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
18	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:99882000-99903000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:99884400-99916000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
22	chr7:99889400-99915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:99890200-99914200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:99890400-99917000	Weak transcription	Fetal Brain Female	brain
25	chr7:99893600-99914200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr7:99893600-99917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:99893600-99917800	Weak transcription	Lung	lung
28	chr7:99893600-99918000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:99896400-99917000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:99896600-99924600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:99896600-99931800	Weak transcription	K562	blood
32	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
33	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
34	chr7:99900200-99902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr7:99901000-99902400	Enhancers	Primary B cells from peripheral blood	blood
36	chr7:99901000-99902400	Enhancers	Fetal Thymus	thymus
37	chr7:99901200-99902400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr7:99901200-99923400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr7:99901600-99902000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:99901600-99902600	Strong transcription	Fetal Stomach	stomach
41	chr7:99901800-99902200	Weak transcription	Thymus	Thymus
42	chr7:99901800-99903200	Strong transcription	Fetal Intestine Small	intestine
43	chr7:99902000-99916800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:99902200-99902400	Enhancers	Thymus	Thymus
45	chr7:99902400-99902600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr7:99902400-99902800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr7:99902400-99914800	Weak transcription	Primary B cells from peripheral blood	blood
48	chr7:99902400-99914800	Weak transcription	Fetal Thymus	thymus
49	chr7:99902400-99915000	Weak transcription	Thymus	Thymus
50	chr7:99902600-99904600	Weak transcription	Fetal Stomach	stomach

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