Variant report

Variant	esv1823451
Chromosome Location	chr7:99900098-99932328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:490)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:99900718-99901136	GM12878	blood:	n/a	n/a
2	BATF	chr7:99931291-99931464	GM12878	blood:	n/a	n/a
3	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
4	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
5	BATF	chr7:99901285-99901496	GM12878	blood:	n/a	n/a
6	BATF	chr7:99922916-99923120	GM12878	blood:	n/a	n/a
7	BATF	chr7:99901300-99901503	GM12878	blood:	n/a	n/a
8	BATF	chr7:99931763-99932072	GM12878	blood:	n/a	n/a
9	BATF	chr7:99902780-99903057	GM12878	blood:	n/a	n/a
10	BATF	chr7:99902062-99903018	GM12878	blood:	n/a	n/a
11	BATF	chr7:99902075-99902343	GM12878	blood:	n/a	n/a
12	BATF	chr7:99902374-99902726	GM12878	blood:	n/a	n/a
13	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
14	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
15	BATF	chr7:99900740-99901050	GM12878	blood:	n/a	n/a
16	BATF	chr7:99931789-99932008	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:99931278-99931549	GM12878	blood:	n/a	chr7:99931369-99931378
19	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
20	BCL11A	chr7:99931290-99931519	GM12878	blood:	n/a	chr7:99931369-99931378
21	BCL11A	chr7:99922866-99923130	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:99901627-99901859	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:99900777-99901048	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:99900720-99901137	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99902084-99902502	GM12878	blood:	n/a	chr7:99902302-99902311
26	BCL11A	chr7:99929074-99929275	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:99922824-99923053	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:99903987-99904347	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
30	BCL11A	chr7:99931741-99932177	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:99931855-99932416	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:99902728-99903004	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
35	BCL11A	chr7:99902046-99902591	GM12878	blood:	n/a	chr7:99902302-99902311
36	BCL11A	chr7:99901601-99901842	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:99918692-99918940	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:99926086-99926279	Hela-S3	cervix:	n/a	chr7:99926106-99926117
39	CEBPB	chr7:99926090-99926280	HepG2	liver:	n/a	chr7:99926106-99926117
40	CEBPB	chr7:99925950-99926249	K562	blood:	n/a	chr7:99926106-99926117
41	CEBPB	chr7:99926091-99926277	IMR90	lung:	n/a	chr7:99926106-99926117
42	CEBPB	chr7:99926097-99926126	K562	blood:	n/a	chr7:99926106-99926117
43	CHD1	chr7:99932051-99932082	GM12878	blood:	n/a	n/a
44	CTCF	chr7:99930547-99930585	GM10266	blood:	n/a	n/a
45	EBF1	chr7:99900664-99901176	GM12878	blood:	n/a	chr7:99900991-99901000
46	EBF1	chr7:99921189-99921874	GM12878	blood:	n/a	n/a
47	EBF1	chr7:99931769-99932106	GM12878	blood:	n/a	n/a
48	EBF1	chr7:99924565-99924827	GM12878	blood:	n/a	n/a
49	EBF1	chr7:99904888-99905056	GM12878	blood:	n/a	n/a
50	EBF1	chr7:99922035-99922479	GM12878	blood:	n/a	chr7:99922279-99922288 chr7:99922279-99922288 chr7:99922278-99922289 chr7:99922279-99922289

(count:490 , 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	H1-hESC	embryonic stem cell:	embryo
2	chr7:99905331-99905381	AG09309	skin:	n/a
3	chr7:99904875-99904925	H1-hESC	embryonic stem cell:	embryo
4	chr7:99905331-99905381	AG09309	skin:	n/a
5	chr7:99929438-99929488	HNPCEpiC	eye:	n/a
6	chr7:99905334-99905384	HCF	heart:	n/a
7	chr7:99905334-99905384	ECC-1	luminal epithelium:	n/a
8	chr7:99929438-99929488	HEEpiC	esophagus:	n/a
9	chr7:99905334-99905384	SKMC	muscle:	n/a
10	chr7:99912131-99912181	HUVEC	blood vessel:	n/a
11	chr7:99912131-99912181	Hela-S3	cervix:	n/a
12	chr7:99932089-99932139	AG04449	skin:	fetal
13	chr7:99912131-99912181	HepG2	liver:	n/a
14	chr7:99904875-99904925	HCT-116	colon:	n/a
15	chr7:99905334-99905384	Caco-2	colon:	n/a
16	chr7:99929438-99929488	HepG2	liver:	n/a
17	chr7:99912131-99912181	BJ	skin:	n/a
18	chr7:99904850-99904900	ProgFib	skin:	n/a
19	chr7:99918120-99918170	HRPEpiC	eye:	n/a
20	chr7:99929438-99929488	HMEC	breast:	n/a
21	chr7:99932089-99932139	MCF-7	breast:	n/a
22	chr7:99912131-99912181	GM19239	blood:	n/a
23	chr7:99904875-99904925	K562	blood:	n/a
24	chr7:99905334-99905384	CMK	blood:	n/a
25	chr7:99929438-99929488	H1-hESC	embryonic stem cell:	embryo
26	chr7:99918120-99918170	AG09309	skin:	n/a
27	chr7:99929438-99929488	Caco-2	colon:	n/a
28	chr7:99932089-99932139	Jurkat	blood:	n/a
29	chr7:99929438-99929488	SKMC	muscle:	n/a
30	chr7:99918120-99918170	SK-N-SH	brain:	n/a
31	chr7:99905334-99905384	PANC-1	pancreas:	n/a
32	chr7:99912131-99912181	HCF	heart:	n/a
33	chr7:99905334-99905384	RPTEC	kidney:	n/a
34	chr7:99912131-99912181	GM12878	blood:	n/a
35	chr7:99905334-99905384	GM12892	blood:	n/a
36	chr7:99932089-99932139	HRCEpiC	kidney:	n/a
37	chr7:99929438-99929488	HRCEpiC	kidney:	n/a
38	chr7:99904850-99904900	K562	blood:	n/a
39	chr7:99904850-99904900	PFSK-1	brain:	n/a
40	chr7:99929438-99929488	IMR90	lung:	fetal
41	chr7:99904850-99904900	HL-60	blood:	n/a
42	chr7:99918120-99918170	MCF-7	breast:	n/a
43	chr7:99905331-99905381	GM12878	blood:	n/a
44	chr7:99912131-99912181	U87	brain:	n/a
45	chr7:99929438-99929488	CMK	blood:	n/a
46	chr7:99912131-99912181	AG04449	skin:	fetal
47	chr7:99929438-99929488	HCPEpiC	choroid plexus:	n/a
48	chr7:99904875-99904925	ECC-1	luminal epithelium:	n/a
49	chr7:99905334-99905384	PrEC	prostate:	n/a
50	chr7:99932089-99932139	HUVEC	blood vessel:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99932234..99937909-chr7:99939373..99942446,6	K562	blood:
2	chr7:99932318..99935048-chr7:100026420..100028378,2	MCF-7	breast:
3	chr7:99931911..99935442-chr7:99938364..99941933,5	MCF-7	breast:

(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-2	chr7:99913916-99914300	expReg_chr7_6439_-
3	lnc-GATS-3	chr7:99928086-99928176	NONHSAT122354
4	lnc-GATS-3	chr7:99927647-99927907	NONHSAT122354

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
ENSG00000146834	chromatin interactions
ENSG00000078319	chromatin interactions
ENSG00000078487	chromatin interactions

Extended variants
information (count: 984 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568351949	chr7:99900150-99900151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535705924	chr7:99900167-99900168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113254600	chr7:99900225-99900226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556997584	chr7:99900260-99900261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537916475	chr7:99900320-99900321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575281635	chr7:99900442-99900443	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377069422	chr7:99900468-99900469	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559285860	chr7:99900471-99900472	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs557549304	chr7:99900487-99900488	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573434242	chr7:99900497-99900498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371038670	chr7:99900590-99900591	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs540461909	chr7:99900669-99900670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562271028	chr7:99900670-99900671	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs202223330	chr7:99900704-99900705	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs573999391	chr7:99900767-99900768	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544475805	chr7:99901018-99901019	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4098888	chr7:99901041-99901042	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs533175968	chr7:99901113-99901114	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs562558335	chr7:99901129-99901130	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs545052988	chr7:99901153-99901154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533141925	chr7:99901191-99901192	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs111475681	chr7:99901192-99901193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs79287945	chr7:99901199-99901200	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs80219228	chr7:99901200-99901201	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs74345635	chr7:99901202-99901203	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs75129765	chr7:99901203-99901204	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs77852455	chr7:99901204-99901205	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs77097872	chr7:99901206-99901207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs80143326	chr7:99901208-99901209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563812647	chr7:99901215-99901216	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs78583505	chr7:99901219-99901220	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76655752	chr7:99901224-99901225	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs75502860	chr7:99901225-99901226	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs77745897	chr7:99901229-99901230	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs74951423	chr7:99901232-99901233	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79085155	chr7:99901234-99901235	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74679972	chr7:99901238-99901239	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs77714252	chr7:99901245-99901246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs186886983	chr7:99901259-99901260	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375693397	chr7:99901278-99901279	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190186026	chr7:99901283-99901284	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs528327122	chr7:99901309-99901310	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs368260553	chr7:99901327-99901328	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546485557	chr7:99901444-99901445	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568212429	chr7:99901494-99901495	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs531001903	chr7:99901532-99901533	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs549601400	chr7:99901555-99901556	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535769453	chr7:99901566-99901567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs550857714	chr7:99901572-99901573	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568903788	chr7:99901598-99901599	Weak transcription Enhancers	TF binding region	1 gene(s)	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:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr7:99870400-99901600	Weak transcription	Thymus	Thymus
4	chr7:99870400-99904600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
9	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:99870600-99904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
13	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr7:99870800-99904600	Weak transcription	Dnd41	blood
16	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
18	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
19	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:99882000-99903000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:99884400-99916000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:99886800-99901600	Weak transcription	Fetal Stomach	stomach
23	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
24	chr7:99889400-99915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:99890200-99914200	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:99890400-99901000	Weak transcription	Fetal Thymus	thymus
27	chr7:99890400-99917000	Weak transcription	Fetal Brain Female	brain
28	chr7:99892800-99901800	Weak transcription	Fetal Intestine Small	intestine
29	chr7:99893600-99914200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr7:99893600-99917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr7:99893600-99917800	Weak transcription	Lung	lung
32	chr7:99893600-99918000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:99896400-99917000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:99896600-99924600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:99896600-99931800	Weak transcription	K562	blood
36	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
37	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
38	chr7:99899200-99901600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:99900200-99902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:99901000-99902400	Enhancers	Primary B cells from peripheral blood	blood
41	chr7:99901000-99902400	Enhancers	Fetal Thymus	thymus
42	chr7:99901200-99902400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr7:99901200-99923400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr7:99901600-99901800	Enhancers	Thymus	Thymus
45	chr7:99901600-99902000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:99901600-99902600	Strong transcription	Fetal Stomach	stomach
47	chr7:99901800-99902200	Weak transcription	Thymus	Thymus
48	chr7:99901800-99903200	Strong transcription	Fetal Intestine Small	intestine
49	chr7:99902000-99916800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:99902200-99902400	Enhancers	Thymus	Thymus

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