Variant report

Variant	esv1849113
Chromosome Location	chr7:38387508-38411786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1532)
CpG islands
(count:488)
Chromatin interactive
region (count:6)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1532 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
2	ATF2	chr7:38409406-38409844	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:38409481-38409625	K562	blood:	n/a	n/a
4	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
5	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
6	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
7	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
8	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
9	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
10	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
11	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
12	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
13	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
14	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
15	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
16	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
17	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
18	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
19	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
20	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
21	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
24	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:38409415-38409953	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
28	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38409538-38409840	K562	blood:	n/a	n/a
31	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
33	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:38409540-38409919	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
36	BRCA1	chr7:38408981-38409171	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
38	CBX3	chr7:38407763-38408208	HCT-116	colon:	n/a	n/a
39	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
40	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
41	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
42	CBX3	chr7:38409444-38409763	K562	blood:	n/a	n/a
43	CBX3	chr7:38407677-38408137	K562	blood:	n/a	n/a
44	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
47	CEBPB	chr7:38407812-38408095	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
49	CHD1	chr7:38407239-38407391	GM12878	blood:	n/a	n/a
50	CHD1	chr7:38389454-38389506	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	chr7:38398839-38398889	HCF	heart:	n/a
2	chr7:38389659-38389709	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:38408106-38408156	HRPEpiC	eye:	n/a
4	chr7:38389685-38389735	AoSMC	blood vessel:	n/a
5	chr7:38398836-38398886	NB4	blood:	n/a
6	chr7:38408106-38408156	Hela-S3	cervix:	n/a
7	chr7:38389659-38389709	ovcar-3	ovarian:	n/a
8	chr7:38389991-38390041	HL-60	blood:	n/a
9	chr7:38403507-38403557	ProgFib	skin:	n/a
10	chr7:38409725-38409775	HRCEpiC	kidney:	n/a
11	chr7:38409725-38409775	HAEpiC	amniotic membrane:	n/a
12	chr7:38389685-38389735	MCF-7	breast:	n/a
13	chr7:38398836-38398886	HRE	kidney:	n/a
14	chr7:38389659-38389709	NB4	blood:	n/a
15	chr7:38408106-38408156	GM06990	blood:	n/a
16	chr7:38389659-38389709	AG04450	lung:	fetal
17	chr7:38403507-38403557	HEEpiC	esophagus:	n/a
18	chr7:38389685-38389735	K562	blood:	n/a
19	chr7:38389991-38390041	ovcar-3	ovarian:	n/a
20	chr7:38389659-38389709	AG10803	skin:	n/a
21	chr7:38398836-38398886	AoSMC	blood vessel:	n/a
22	chr7:38389685-38389735	SK-N-SH_RA	brain:	n/a
23	chr7:38389685-38389735	HL-60	blood:	n/a
24	chr7:38409725-38409775	HEEpiC	esophagus:	n/a
25	chr7:38403507-38403557	PrEC	prostate:	n/a
26	chr7:38389685-38389735	HUVEC	blood vessel:	n/a
27	chr7:38408106-38408156	PFSK-1	brain:	n/a
28	chr7:38408106-38408156	T-47D	breast:	n/a
29	chr7:38403507-38403557	HCM	heart:	n/a
30	chr7:38389685-38389735	AG04450	lung:	fetal
31	chr7:38409725-38409775	SAEC	small airway:	n/a
32	chr7:38389991-38390041	HEK293	kidney:	embryo
33	chr7:38389659-38389709	GM12892	blood:	n/a
34	chr7:38398839-38398889	HL-60	blood:	n/a
35	chr7:38389685-38389735	GM19239	blood:	n/a
36	chr7:38389659-38389709	HCPEpiC	choroid plexus:	n/a
37	chr7:38409725-38409775	NB4	blood:	n/a
38	chr7:38389685-38389735	SAEC	small airway:	n/a
39	chr7:38389991-38390041	AG10803	skin:	n/a
40	chr7:38398836-38398886	HMEC	breast:	n/a
41	chr7:38389991-38390041	AG09309	skin:	n/a
42	chr7:38403507-38403557	CMK	blood:	n/a
43	chr7:38389685-38389735	HepG2	liver:	n/a
44	chr7:38409725-38409775	AG09319	gingival:	n/a
45	chr7:38389685-38389735	U87	brain:	n/a
46	chr7:38389991-38390041	A549	lung:	n/a
47	chr7:38403507-38403557	NB4	blood:	n/a
48	chr7:38389991-38390041	HAEpiC	amniotic membrane:	n/a
49	chr7:38398839-38398889	AG04450	lung:	fetal
50	chr7:38398839-38398889	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
2	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
3	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
4	chr7:38409691..38411244-chr7:38417623..38419459,2	K562	blood:
5	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
6	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
2	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
3	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
4	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
5	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
6	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
7	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
8	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
9	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
10	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
11	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179

No data

Variant related genes	Relation type
TRGV2	TF binding region
TRGV5	TF binding region
TRGV1	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
TRGV5	CpG island
TRGV1	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV5P	CpG island
ENSG00000226212	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000249978	chromatin interactions
RAB5A	miRNA target sites

Extended variants
information (count: 1509 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148545430	chr7:38387509-38387510	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141814580	chr7:38387511-38387512	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189417133	chr7:38387520-38387521	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs56242205	chr7:38387548-38387549	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
5	rs375438635	chr7:38387565-38387566	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181976615	chr7:38387571-38387572	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537857646	chr7:38387574-38387575	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554886830	chr7:38387583-38387584	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386712325	chr7:38387610-38387611	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189089003	chr7:38387611-38387612	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542104428	chr7:38387621-38387622	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555789039	chr7:38387629-38387630	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372567652	chr7:38387631-38387632	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553724286	chr7:38387638-38387639	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576975000	chr7:38387643-38387644	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545050937	chr7:38387644-38387645	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558646926	chr7:38387653-38387654	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530786655	chr7:38387692-38387693	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575613403	chr7:38387695-38387696	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374685362	chr7:38387701-38387702	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544229267	chr7:38387713-38387714	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs2534590	chr7:38387731-38387732	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs530370720	chr7:38387739-38387740	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373442378	chr7:38387754-38387755	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181121352	chr7:38387762-38387763	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2736946	chr7:38387763-38387764	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs144946632	chr7:38387769-38387770	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369928078	chr7:38387775-38387776	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552268852	chr7:38387787-38387788	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569006112	chr7:38387803-38387804	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531310546	chr7:38387823-38387824	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs57798381	chr7:38387824-38387825	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568335047	chr7:38387858-38387859	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140067125	chr7:38387859-38387860	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554035372	chr7:38387908-38387909	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377732398	chr7:38387911-38387912	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539263279	chr7:38387912-38387913	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558606353	chr7:38387934-38387935	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77084610	chr7:38387941-38387942	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56284498	chr7:38387967-38387968	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536534548	chr7:38387971-38387972	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs544191130	chr7:38387989-38387990	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs28504113	chr7:38387992-38387993	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2534591	chr7:38387995-38387996	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149062173	chr7:38388033-38388034	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs13309318	chr7:38388066-38388067	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11761741	chr7:38388094-38388095	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs560857399	chr7:38388109-38388110	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532739320	chr7:38388112-38388113	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs13309373	chr7:38388115-38388116	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
3	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
4	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
6	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:38384800-38390800	Active TSS	Thymus	Thymus
8	chr7:38385000-38388800	Weak transcription	Spleen	Spleen
9	chr7:38385600-38389000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
13	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr7:38386000-38388600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:38386000-38388600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:38386000-38388800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
19	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:38386000-38389200	Weak transcription	K562	blood
23	chr7:38386200-38388200	Enhancers	Dnd41	blood
24	chr7:38386200-38388600	Weak transcription	Fetal Thymus	thymus
25	chr7:38386800-38387800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:38386800-38388400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
28	chr7:38387000-38387600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:38387400-38387800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr7:38387400-38388000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr7:38387400-38388200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:38387600-38388000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:38387800-38388200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:38387800-38388800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr7:38388000-38388200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:38388000-38388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:38388200-38388600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:38388200-38388800	Weak transcription	Dnd41	blood
40	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:38388200-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr7:38388400-38388800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr7:38388400-38389200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:38388600-38389000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:38388600-38389200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr7:38388600-38390200	Flanking Active TSS	Fetal Thymus	thymus
47	chr7:38388600-38390400	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr7:38388600-38391000	Enhancers	Primary B cells from peripheral blood	blood
49	chr7:38388800-38389000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr7:38388800-38389200	Active TSS	Dnd41	blood

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