Variant report

Variant	esv1815812
Chromosome Location	chr7:99874387-99930879
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:99889833-99890086	GM12878	blood:	n/a	n/a
2	BATF	chr7:99902062-99903018	GM12878	blood:	n/a	n/a
3	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
4	BATF	chr7:99902780-99903057	GM12878	blood:	n/a	n/a
5	BATF	chr7:99902374-99902726	GM12878	blood:	n/a	n/a
6	BATF	chr7:99902075-99902343	GM12878	blood:	n/a	n/a
7	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
8	BATF	chr7:99901285-99901496	GM12878	blood:	n/a	n/a
9	BATF	chr7:99889728-99890156	GM12878	blood:	n/a	n/a
10	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
11	BATF	chr7:99922916-99923120	GM12878	blood:	n/a	n/a
12	BATF	chr7:99900740-99901050	GM12878	blood:	n/a	n/a
13	BATF	chr7:99901300-99901503	GM12878	blood:	n/a	n/a
14	BATF	chr7:99889699-99890163	GM12878	blood:	n/a	n/a
15	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
16	BATF	chr7:99900718-99901136	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:99922866-99923130	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
19	BCL11A	chr7:99899365-99899765	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:99901627-99901859	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:99900777-99901048	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:99900720-99901137	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:99889658-99890197	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99902728-99903004	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:99902084-99902502	GM12878	blood:	n/a	chr7:99902302-99902311
27	BCL11A	chr7:99899420-99899769	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:99903987-99904347	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
30	BCL11A	chr7:99889722-99890078	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:99902046-99902591	GM12878	blood:	n/a	chr7:99902302-99902311
33	BCL11A	chr7:99922824-99923053	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
35	BCL11A	chr7:99901601-99901842	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:99929074-99929275	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:99918692-99918940	HepG2	liver:	n/a	n/a
38	CBX3	chr7:99889691-99890054	K562	blood:	n/a	n/a
39	CEBPB	chr7:99882137-99882255	K562	blood:	n/a	chr7:99882189-99882200
40	CEBPB	chr7:99893016-99893151	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:99925950-99926249	K562	blood:	n/a	chr7:99926106-99926117
42	CEBPB	chr7:99926097-99926126	K562	blood:	n/a	chr7:99926106-99926117
43	CEBPB	chr7:99882111-99882313	A549	lung:	n/a	chr7:99882189-99882200
44	CEBPB	chr7:99926086-99926279	Hela-S3	cervix:	n/a	chr7:99926106-99926117
45	CEBPB	chr7:99926091-99926277	IMR90	lung:	n/a	chr7:99926106-99926117
46	CEBPB	chr7:99926090-99926280	HepG2	liver:	n/a	chr7:99926106-99926117
47	CEBPB	chr7:99882132-99882257	HepG2	liver:	n/a	chr7:99882189-99882200
48	CEBPB	chr7:99882084-99882308	IMR90	lung:	n/a	chr7:99882189-99882200
49	CTCF	chr7:99874487-99874582	Lung_OC	lung:	n/a	n/a
50	CTCF	chr7:99930547-99930585	GM10266	blood:	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	chr7:99918120-99918170	SK-N-SH	brain:	n/a
2	chr7:99918120-99918170	HepG2	liver:	n/a
3	chr7:99905334-99905384	AG09309	skin:	n/a
4	chr7:99905331-99905381	GM12892	blood:	n/a
5	chr7:99912131-99912181	HCT-116	colon:	n/a
6	chr7:99905331-99905381	HNPCEpiC	eye:	n/a
7	chr7:99912131-99912181	HRE	kidney:	n/a
8	chr7:99929438-99929488	GM12878	blood:	n/a
9	chr7:99904850-99904900	HRCEpiC	kidney:	n/a
10	chr7:99904850-99904900	ovcar-3	ovarian:	n/a
11	chr7:99912131-99912181	LNCaP	prostate:	n/a
12	chr7:99905331-99905381	BE2_C	brain:	n/a
13	chr7:99918120-99918170	AG04450	lung:	fetal
14	chr7:99905331-99905381	PrEC	prostate:	n/a
15	chr7:99904850-99904900	HNPCEpiC	eye:	n/a
16	chr7:99905331-99905381	ECC-1	luminal epithelium:	n/a
17	chr7:99904850-99904900	HepG2	liver:	n/a
18	chr7:99905334-99905384	H1-hESC	embryonic stem cell:	embryo
19	chr7:99918120-99918170	SK-N-SH_RA	brain:	n/a
20	chr7:99904850-99904900	HCPEpiC	choroid plexus:	n/a
21	chr7:99905331-99905381	LNCaP	prostate:	n/a
22	chr7:99904875-99904925	Caco-2	colon:	n/a
23	chr7:99905331-99905381	HUVEC	blood vessel:	n/a
24	chr7:99904875-99904925	AG09319	gingival:	n/a
25	chr7:99905331-99905381	A549	lung:	n/a
26	chr7:99912131-99912181	HUVEC	blood vessel:	n/a
27	chr7:99912131-99912181	GM12878	blood:	n/a
28	chr7:99929438-99929488	PANC-1	pancreas:	n/a
29	chr7:99918120-99918170	HRCEpiC	kidney:	n/a
30	chr7:99904875-99904925	AoSMC	blood vessel:	n/a
31	chr7:99929438-99929488	RPTEC	kidney:	n/a
32	chr7:99929438-99929488	HL-60	blood:	n/a
33	chr7:99904850-99904900	HRPEpiC	eye:	n/a
34	chr7:99904850-99904900	NT2-D1	testis:	n/a
35	chr7:99904875-99904925	LNCaP	prostate:	n/a
36	chr7:99904850-99904900	HAEpiC	amniotic membrane:	n/a
37	chr7:99904875-99904925	CMK	blood:	n/a
38	chr7:99905334-99905384	NT2-D1	testis:	n/a
39	chr7:99905334-99905384	GM12891	blood:	n/a
40	chr7:99912131-99912181	HAEpiC	amniotic membrane:	n/a
41	chr7:99904850-99904900	HL-60	blood:	n/a
42	chr7:99918120-99918170	AG10803	skin:	n/a
43	chr7:99912131-99912181	Caco-2	colon:	n/a
44	chr7:99904850-99904900	PANC-1	pancreas:	n/a
45	chr7:99904875-99904925	NHDF-neo	bronchial:	n/a
46	chr7:99905334-99905384	AG09319	gingival:	n/a
47	chr7:99912131-99912181	PFSK-1	brain:	n/a
48	chr7:99904850-99904900	ProgFib	skin:	n/a
49	chr7:99929438-99929488	MCF-7	breast:	n/a
50	chr7:99904875-99904925	H1-hESC	embryonic stem cell:	embryo

No data

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

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

No data

Variant related genes	Relation type
PMS2P1	TF binding region
ENSG00000239521	TF binding region
ENSG00000201913	TF binding region
STAG3L5P	TF binding region
GATS	TF binding region
PILRB	TF binding region
SPDYE3	TF binding region
STAG3L5P-PVRIG2P-PILRB	TF binding region
PMS2P1	CpG island
ENSG00000239521	CpG island
ENSG00000201913	CpG island
STAG3L5P	CpG island
GATS	CpG island
PILRB	CpG island
SPDYE3	CpG island
STAG3L5P-PVRIG2P-PILRB	CpG island

Extended variants
information (count: 1746 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372810742	chr7:99874487-99874488	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs540391123	chr7:99874513-99874514	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs574807037	chr7:99874564-99874565	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs551809044	chr7:99874681-99874682	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs145160342	chr7:99874690-99874691	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs144938209	chr7:99874695-99874696	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs541618868	chr7:99874730-99874731	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs200257160	chr7:99874790-99874791	Weak transcription Enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs563291362	chr7:99874892-99874893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35471830	chr7:99874902-99874903	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530694882	chr7:99874968-99874969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149096288	chr7:99874978-99874979	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117244534	chr7:99874997-99874998	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200132253	chr7:99875029-99875030	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192147658	chr7:99875079-99875080	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546726113	chr7:99875100-99875101	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10085453	chr7:99875114-99875115	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568151758	chr7:99875126-99875127	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540602193	chr7:99875133-99875134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372752126	chr7:99875155-99875156	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111638574	chr7:99875175-99875176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184296139	chr7:99875278-99875279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551170778	chr7:99875285-99875286	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201095022	chr7:99875303-99875304	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62482193	chr7:99875335-99875336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569566137	chr7:99875346-99875347	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375991404	chr7:99875403-99875404	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182886074	chr7:99875484-99875485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566757200	chr7:99875568-99875569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534158096	chr7:99875569-99875570	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555483667	chr7:99875572-99875573	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4729582	chr7:99875694-99875695	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs187836866	chr7:99875706-99875707	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145521424	chr7:99875736-99875737	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117598157	chr7:99875738-99875739	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545802530	chr7:99875774-99875775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564363386	chr7:99875781-99875782	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568244843	chr7:99875838-99875839	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376877231	chr7:99875847-99875848	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528114676	chr7:99875900-99875901	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371449567	chr7:99875904-99875905	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192950783	chr7:99876004-99876005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184254906	chr7:99876005-99876006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138235358	chr7:99876010-99876011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4729583	chr7:99876059-99876060	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374182957	chr7:99876100-99876101	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368898944	chr7:99876106-99876107	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35591576	chr7:99876107-99876108	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199951033	chr7:99876109-99876110	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371165331	chr7:99876110-99876111	Weak transcription Enhancers Strong 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
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99880600	Weak transcription	Fetal Lung	lung
2	chr7:99870200-99884200	Weak transcription	Aorta	Aorta
3	chr7:99870200-99916800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:99870200-99932800	Weak transcription	Ovary	ovary
5	chr7:99870400-99876800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:99870400-99885000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:99870400-99886200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:99870400-99901600	Weak transcription	Thymus	Thymus
9	chr7:99870400-99904600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
12	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
14	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:99870600-99874800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:99870600-99879800	Weak transcription	A549	lung
17	chr7:99870600-99880800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:99870600-99886400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:99870600-99887800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:99870600-99888400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:99870600-99888600	Weak transcription	GM12878-XiMat	blood
22	chr7:99870600-99890000	Weak transcription	Fetal Thymus	thymus
23	chr7:99870600-99898800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr7:99870600-99904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
27	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:99870800-99882400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:99870800-99904600	Weak transcription	Dnd41	blood
31	chr7:99871000-99886200	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
34	chr7:99873400-99876000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:99873400-99876200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr7:99873600-99877800	Strong transcription	Fetal Stomach	stomach
37	chr7:99874000-99875800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:99874000-99878000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr7:99874200-99879000	Weak transcription	Fetal Intestine Small	intestine
40	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
41	chr7:99875800-99877800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:99875800-99879400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:99876000-99881000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:99877800-99883600	Weak transcription	Fetal Stomach	stomach
45	chr7:99877800-99883800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:99879000-99879800	Strong transcription	Fetal Intestine Small	intestine
47	chr7:99879800-99883800	Weak transcription	Fetal Intestine Small	intestine
48	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr7:99880800-99881200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:99881000-99882000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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