Variant report

Variant	nsv962986
Chromosome Location	chr19:42073874-42080172
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCLAF1	chr19:42076940-42077340	GM12878	blood:	n/a	n/a
2	BHLHE40	chr19:42077015-42077237	GM12878	blood:	n/a	n/a
3	BHLHE40	chr19:42077052-42077252	K562	blood:	n/a	n/a
4	BRCA1	chr19:42077105-42077179	GM12878	blood:	n/a	n/a
5	CHD2	chr19:42077159-42077169	HepG2	liver:	n/a	n/a
6	CTCF	chr19:42077120-42077270	HFF	foreskin:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
7	CTCF	chr19:42077100-42077250	AG09319	gingival:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
8	CTCF	chr19:42077403-42077502	MCF-7	breast:	n/a	n/a
9	CTCF	chr19:42077760-42077910	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr19:42077032-42077294	Pancreas_OC	pancreas:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
11	CTCF	chr19:42076620-42076770	GM12872	blood:	n/a	n/a
12	CTCF	chr19:42077100-42077250	AoAF	blood vessel:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
13	CTCF	chr19:42077060-42077210	GM12874	blood:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
14	CTCF	chr19:42077520-42077670	NHLF	lung:	n/a	n/a
15	CTCF	chr19:42076672-42076921	GM19238	blood:	n/a	n/a
16	CTCF	chr19:42077402-42077471	NHEK	skin:	n/a	n/a
17	CTCF	chr19:42077120-42077270	NB4	blood:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
18	CTCF	chr19:42076681-42076791	HepG2	liver:	n/a	n/a
19	CTCF	chr19:42076404-42076412	Fibrobl	skin:	n/a	n/a
20	CTCF	chr19:42077100-42077250	HEEpiC	esophagus:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
21	CTCF	chr19:42076680-42076830	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:42076487-42077444	MCF-7	breast:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
23	CTCF	chr19:42076639-42076851	MCF-7	breast:	n/a	n/a
24	CTCF	chr19:42077120-42077270	HMEC	breast:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
25	CTCF	chr19:42076620-42076770	GM12875	blood:	n/a	n/a
26	CTCF	chr19:42077020-42077170	WI-38	lung:	n/a	chr19:42077161-42077169
27	CTCF	chr19:42076660-42076810	GM12864	blood:	n/a	n/a
28	CTCF	chr19:42076640-42076777	HepG2	liver:	n/a	n/a
29	CTCF	chr19:42077014-42077309	K562	blood:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
30	CTCF	chr19:42076680-42076830	GM12864	blood:	n/a	n/a
31	CTCF	chr19:42076640-42076790	GM12866	blood:	n/a	n/a
32	CTCF	chr19:42077395-42077525	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:42077100-42077250	AG09309	skin:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
34	CTCF	chr19:42076320-42076507	MCF-7	breast:	n/a	chr19:42076414-42076427 chr19:42076411-42076424 chr19:42076411-42076429
35	CTCF	chr19:42077036-42077326	GM10266	blood:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
36	CTCF	chr19:42077012-42077337	NHEK	skin:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
37	CTCF	chr19:42076921-42077320	H1-hESC	embryonic stem cell:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
38	CTCF	chr19:42077100-42077250	GM12871	blood:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
39	CTCF	chr19:42076791-42076792	GM10266	blood:	n/a	n/a
40	CTCF	chr19:42077100-42077250	AG04450	lung:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
41	CTCF	chr19:42077080-42077230	HMF	breast:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
42	CTCF	chr19:42076956-42077551	Gliobla	brain:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
43	CTCF	chr19:42077100-42077250	HPAF	blood vessel:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
44	CTCF	chr19:42077120-42077270	Hela-S3	cervix:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
45	CTCF	chr19:42077029-42077285	HepG2	liver:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
46	CTCF	chr19:42076963-42077238	T-47D	breast:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
47	CTCF	chr19:42077033-42077302	Kidney_OC	kidney:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
48	CTCF	chr19:42077080-42077230	AG09319	gingival:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077161-42077169
49	CTCF	chr19:42076487-42077435	HCT-116	colon:	n/a	chr19:42077151-42077172 chr19:42077156-42077174 chr19:42077158-42077171 chr19:42077157-42077173 chr19:42077014-42077027 chr19:42077161-42077169
50	CTCF	chr19:42076620-42076770	GM12866	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41959542..41961581-chr19:42071875..42074732,2	K562	blood:
2	chr19:42078682..42081058-chr19:42082951..42085705,2	MCF-7	breast:
3	chr19:41877183..41879193-chr19:42077275..42079730,2	MCF-7	breast:
4	chr19:41945498..41946299-chr19:42076700..42077272,2	MCF-7	breast:
5	chr19:41953484..41955550-chr19:42076712..42078351,2	MCF-7	breast:
6	chr19:42044232..42044742-chr19:42076655..42077555,2	MCF-7	breast:
7	chr19:42048109..42049006-chr19:42076514..42077838,6	MCF-7	breast:
8	chr19:42048016..42049035-chr19:42076640..42077541,6	MCF-7	breast:
9	chr19:41943990..41946987-chr19:42072423..42074173,2	K562	blood:
10	chr19:41954980..41955905-chr19:42076786..42077640,5	K562	blood:
11	chr19:41954991..41955547-chr19:42076737..42077301,2	MCF-7	breast:
12	chr19:41941738..41942622-chr19:42076685..42077563,3	MCF-7	breast:
13	chr19:41954976..41956003-chr19:42076182..42077940,10	MCF-7	breast:
14	chr19:41824418..41826193-chr19:42074523..42077074,2	K562	blood:
15	chr19:42069422..42070951-chr19:42073170..42075974,2	MCF-7	breast:
16	chr19:42077943..42079577-chr19:42084170..42086427,2	K562	blood:

Variant related genes	Relation type
CEACAM21	TF binding region
ENSG00000105341	chromatin interactions
ENSG00000142039	chromatin interactions

Extended variants
information (count: 239 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:239 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187258979	chr19:42073887-42073888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141857707	chr19:42073892-42073893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577895026	chr19:42073893-42073894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544894311	chr19:42073913-42073914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191883086	chr19:42073930-42073931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372261247	chr19:42074034-42074035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527296623	chr19:42074149-42074150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs8100158	chr19:42074165-42074166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533991345	chr19:42074169-42074170	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531411367	chr19:42074179-42074180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550926296	chr19:42074224-42074225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540086516	chr19:42074242-42074243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539790190	chr19:42074250-42074251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35461515	chr19:42074253-42074254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs57600815	chr19:42074254-42074255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs397717435	chr19:42074269-42074270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374053245	chr19:42074356-42074357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552105270	chr19:42074479-42074480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567129498	chr19:42074495-42074496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184076533	chr19:42074550-42074551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553295306	chr19:42074570-42074571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573464651	chr19:42074571-42074572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189354065	chr19:42074581-42074582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192686022	chr19:42074601-42074602	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146053374	chr19:42074604-42074605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550640396	chr19:42074607-42074608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577767142	chr19:42074623-42074624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568961343	chr19:42074626-42074627	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373646857	chr19:42074654-42074655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544760713	chr19:42074705-42074706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368744057	chr19:42074772-42074773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs62119420	chr19:42074773-42074774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs571978242	chr19:42074830-42074831	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559765481	chr19:42074853-42074854	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377723042	chr19:42074874-42074875	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35657165	chr19:42074906-42074907	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376358219	chr19:42074943-42074944	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542240638	chr19:42075013-42075014	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75917800	chr19:42075035-42075036	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs62119421	chr19:42075036-42075037	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs76369648	chr19:42075060-42075061	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139982136	chr19:42075079-42075080	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564780583	chr19:42075085-42075086	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377407532	chr19:42075150-42075151	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533574915	chr19:42075188-42075189	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545029275	chr19:42075199-42075200	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551970300	chr19:42075209-42075210	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567193934	chr19:42075241-42075242	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534473495	chr19:42075271-42075272	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143445418	chr19:42075280-42075281	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Schizophrenia	18511947	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42069400-42077600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr19:42071400-42074600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr19:42071400-42076400	Weak transcription	GM12878-XiMat	blood
4	chr19:42071600-42076400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr19:42071600-42082000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr19:42072000-42074200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr19:42072000-42074200	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr19:42072000-42075000	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr19:42072400-42074800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr19:42072400-42076600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr19:42072600-42074800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr19:42072800-42078600	Weak transcription	Primary B cells from cord blood	blood
13	chr19:42073000-42074000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:42073000-42074800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr19:42073000-42076600	Weak transcription	Primary T cells from cord blood	blood
16	chr19:42073200-42074800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr19:42073200-42076400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:42073600-42074000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr19:42073800-42074200	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr19:42073800-42074800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr19:42073800-42075200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr19:42073800-42075600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:42074000-42076000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr19:42074000-42076400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr19:42074200-42074600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr19:42074200-42076000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr19:42074600-42075000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr19:42074600-42075600	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr19:42074800-42075000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr19:42074800-42075200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr19:42074800-42075200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr19:42074800-42075200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr19:42074800-42077600	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr19:42075000-42075200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr19:42075000-42075200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr19:42075000-42075400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
37	chr19:42075200-42075400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr19:42075200-42076000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr19:42075200-42076000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr19:42075200-42076400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr19:42075200-42076400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr19:42075200-42076400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr19:42075400-42076000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr19:42075400-42077800	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr19:42075600-42076200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
46	chr19:42075600-42076400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr19:42076000-42076400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:42076000-42076600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr19:42076000-42077400	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr19:42076000-42077400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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