Variant report

Variant	nsv1013200
Chromosome Location	chr1:168332730-168357759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:491)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168343229-168343407	K562	blood:	n/a	n/a
2	ARID3A	chr1:168335503-168335579	K562	blood:	n/a	n/a
3	ARID3A	chr1:168335006-168335245	K562	blood:	n/a	n/a
4	ARID3A	chr1:168337311-168337679	HepG2	liver:	n/a	n/a
5	ATF1	chr1:168342118-168342700	K562	blood:	n/a	n/a
6	ATF1	chr1:168341584-168341901	K562	blood:	n/a	n/a
7	ATF1	chr1:168335008-168335286	K562	blood:	n/a	n/a
8	ATF1	chr1:168343203-168343424	K562	blood:	n/a	n/a
9	ATF2	chr1:168356361-168357102	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
10	ATF2	chr1:168356434-168356843	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
11	ATF3	chr1:168355801-168356057	K562	blood:	n/a	n/a
12	ATF3	chr1:168343126-168343426	K562	blood:	n/a	n/a
13	BACH1	chr1:168356174-168356821	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:168334918-168335322	K562	blood:	n/a	n/a
15	BACH1	chr1:168357056-168357360	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr1:168348281-168348839	A549	lung:	n/a	chr1:168348563-168348572 chr1:168348562-168348571
17	BHLHE40	chr1:168341818-168342686	K562	blood:	n/a	n/a
18	BHLHE40	chr1:168347732-168348156	K562	blood:	n/a	n/a
19	BHLHE40	chr1:168338996-168339285	K562	blood:	n/a	n/a
20	BHLHE40	chr1:168343187-168343406	K562	blood:	n/a	n/a
21	BHLHE40	chr1:168335065-168335538	K562	blood:	n/a	n/a
22	BRCA1	chr1:168356568-168356732	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr1:168334932-168335691	K562	blood:	n/a	n/a
24	CBX3	chr1:168341561-168342695	K562	blood:	n/a	n/a
25	CCNT2	chr1:168342245-168342534	K562	blood:	n/a	n/a
26	CCNT2	chr1:168356471-168356697	K562	blood:	n/a	n/a
27	CCNT2	chr1:168343207-168343407	K562	blood:	n/a	n/a
28	CEBPB	chr1:168335183-168335345	K562	blood:	n/a	n/a
29	CEBPB	chr1:168351108-168351470	K562	blood:	n/a	chr1:168351297-168351308
30	CEBPB	chr1:168348401-168348826	A549	lung:	n/a	n/a
31	CEBPB	chr1:168348327-168348851	A549	lung:	n/a	n/a
32	CEBPB	chr1:168351164-168351466	A549	lung:	n/a	chr1:168351297-168351308
33	CEBPB	chr1:168348447-168348725	A549	lung:	n/a	n/a
34	CEBPB	chr1:168335571-168335717	K562	blood:	n/a	n/a
35	CEBPB	chr1:168342049-168342676	K562	blood:	n/a	n/a
36	CEBPB	chr1:168351157-168351436	IMR90	lung:	n/a	chr1:168351297-168351308
37	CEBPB	chr1:168351157-168351490	HepG2	liver:	n/a	chr1:168351297-168351308
38	CEBPB	chr1:168348425-168348794	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:168337399-168337680	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:168353959-168354079	K562	blood:	n/a	n/a
41	CEBPB	chr1:168343818-168344162	K562	blood:	n/a	n/a
42	CEBPD	chr1:168342121-168342789	K562	blood:	n/a	n/a
43	CEBPD	chr1:168342091-168342677	K562	blood:	n/a	n/a
44	CEBPZ	chr1:168337441-168337505	HepG2	liver:	n/a	n/a
45	CHD2	chr1:168335269-168335352	K562	blood:	n/a	n/a
46	CHD2	chr1:168356478-168357380	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr1:168356468-168356842	GM12878	blood:	n/a	chr1:168356576-168356589
48	CREB1	chr1:168356449-168356702	A549	lung:	n/a	chr1:168356576-168356589
49	CREB1	chr1:168356418-168356833	H1-hESC	embryonic stem cell:	n/a	chr1:168356576-168356589
50	CREB1	chr1:168356264-168356908	H1-hESC	embryonic stem cell:	n/a	chr1:168356576-168356589

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168344264-168344314	HMEC	breast:	n/a
2	chr1:168356537-168356587	MCF-7	breast:	n/a
3	chr1:168343339-168343389	PANC-1	pancreas:	n/a
4	chr1:168344264-168344314	HMEC	breast:	n/a
5	chr1:168356537-168356587	MCF-7	breast:	n/a
6	chr1:168343339-168343389	PANC-1	pancreas:	n/a
7	chr1:168343945-168343995	AG04450	lung:	fetal
8	chr1:168344184-168344234	HCT-116	colon:	n/a
9	chr1:168356537-168356587	SK-N-MC	brain:	n/a
10	chr1:168344184-168344234	NT2-D1	testis:	n/a
11	chr1:168356673-168356723	HL-60	blood:	n/a
12	chr1:168344184-168344234	NHDF-neo	bronchial:	n/a
13	chr1:168356673-168356723	AG04450	lung:	fetal
14	chr1:168356673-168356723	LNCaP	prostate:	n/a
15	chr1:168356591-168356641	AG04450	lung:	fetal
16	chr1:168344264-168344314	HAEpiC	amniotic membrane:	n/a
17	chr1:168356537-168356587	PFSK-1	brain:	n/a
18	chr1:168356537-168356587	A549	lung:	n/a
19	chr1:168344264-168344314	RPTEC	kidney:	n/a
20	chr1:168356591-168356641	Hepatocyte	liver:	n/a
21	chr1:168344264-168344314	HEK293	kidney:	embryo
22	chr1:168343945-168343995	ProgFib	skin:	n/a
23	chr1:168343339-168343389	HCF	heart:	n/a
24	chr1:168356606-168356656	HEK293	kidney:	embryo
25	chr1:168356606-168356656	AoSMC	blood vessel:	n/a
26	chr1:168356591-168356641	GM12892	blood:	n/a
27	chr1:168356673-168356723	HIPEpiC	eye:	n/a
28	chr1:168343945-168343995	HEK293	kidney:	embryo
29	chr1:168356537-168356587	H1-hESC	embryonic stem cell:	embryo
30	chr1:168356591-168356641	AG10803	skin:	n/a
31	chr1:168344264-168344314	SK-N-MC	brain:	n/a
32	chr1:168343945-168343995	AG04449	skin:	fetal
33	chr1:168356591-168356641	HIPEpiC	eye:	n/a
34	chr1:168343945-168343995	K562	blood:	n/a
35	chr1:168343945-168343995	NHBE	bronchial:	n/a
36	chr1:168356591-168356641	SAEC	small airway:	n/a
37	chr1:168356606-168356656	T-47D	breast:	n/a
38	chr1:168356537-168356587	Hela-S3	cervix:	n/a
39	chr1:168356537-168356587	SK-N-SH_RA	brain:	n/a
40	chr1:168356606-168356656	Hela-S3	cervix:	n/a
41	chr1:168344264-168344314	CMK	blood:	n/a
42	chr1:168343945-168343995	ovcar-3	ovarian:	n/a
43	chr1:168356591-168356641	HRCEpiC	kidney:	n/a
44	chr1:168356673-168356723	A549	lung:	n/a
45	chr1:168343945-168343995	BE2_C	brain:	n/a
46	chr1:168356537-168356587	HEEpiC	esophagus:	n/a
47	chr1:168343945-168343995	HNPCEpiC	eye:	n/a
48	chr1:168356606-168356656	HepG2	liver:	n/a
49	chr1:168356606-168356656	BE2_C	brain:	n/a
50	chr1:168343339-168343389	HRPEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
2	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:
3	chr1:168187433..168189118-chr1:168341371..168344286,2	K562	blood:
4	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
5	chr1:168333149..168334696-chr1:168337018..168339175,2	K562	blood:
6	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
7	chr1:168311877..168312534-chr1:168334700..168335638,2	K562	blood:
8	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
9	chr1:168328202..168331069-chr1:168335120..168337354,2	K562	blood:
10	chr1:168311615..168313900-chr1:168348090..168350975,2	MCF-7	breast:
11	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
12	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
13	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
14	chr1:168311666..168312512-chr1:168334779..168335573,2	MCF-7	breast:
15	chr1:168312661..168313699-chr1:168334688..168335805,3	K562	blood:
16	chr1:168355026..168356826-chr1:168398882..168401309,2	K562	blood:
17	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
18	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
19	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
20	chr1:168334562..168336538-chr1:168357801..168359534,2	K562	blood:
21	chr1:168343623..168346188-chr1:168350297..168353036,3	K562	blood:
22	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
23	chr1:168311676..168312490-chr1:168334705..168335594,4	MCF-7	breast:
24	chr1:168344082..168345767-chr1:168346742..168349715,2	K562	blood:
25	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
26	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
27	chr1:168311642..168312682-chr1:168331951..168332907,6	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-557	chr1:168344822-168344844	MIMAT0003221

No data

Variant related genes	Relation type
MIR557	TF binding region
ENSG00000227722	TF binding region
MIR557	CpG island
ENSG00000227722	CpG island
ENSG00000227722	chromatin interactions
ENSG00000207974	chromatin interactions

Extended variants
information (count: 933 )
Associated
traits (count: 93 )

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	rs2223293	chr1:168332730-168332731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1886004	chr1:168332753-168332754	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191676197	chr1:168332769-168332770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535443270	chr1:168332785-168332786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557639709	chr1:168332794-168332795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555031204	chr1:168332818-168332819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575505730	chr1:168332820-168332821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539661071	chr1:168332865-168332866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75273172	chr1:168332878-168332879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184016208	chr1:168332886-168332887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142049905	chr1:168332896-168332897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187250893	chr1:168332941-168332942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574383292	chr1:168332996-168332997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76371748	chr1:168333000-168333001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58440761	chr1:168333010-168333011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558359874	chr1:168333085-168333086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12123087	chr1:168333125-168333126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs117428357	chr1:168333145-168333146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115661207	chr1:168333198-168333199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373407525	chr1:168333240-168333241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140297797	chr1:168333245-168333246	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547082913	chr1:168333288-168333289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544117091	chr1:168333327-168333328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372725923	chr1:168333410-168333411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529312130	chr1:168333485-168333486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192940867	chr1:168333489-168333490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569245803	chr1:168333491-168333492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539462301	chr1:168333530-168333531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557976722	chr1:168333604-168333605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144017066	chr1:168333657-168333658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563182304	chr1:168333660-168333661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs79672379	chr1:168333729-168333730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185386348	chr1:168333758-168333759	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190320736	chr1:168333770-168333771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376407044	chr1:168333783-168333784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551735883	chr1:168333800-168333801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556977329	chr1:168333809-168333810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575636605	chr1:168333814-168333815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182560973	chr1:168333816-168333817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574779480	chr1:168333834-168333835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528294245	chr1:168333835-168333836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540026981	chr1:168333872-168333873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370096171	chr1:168333895-168333896	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562227376	chr1:168333913-168333914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559371397	chr1:168333917-168333918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550981142	chr1:168333930-168333931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568909040	chr1:168333960-168333961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533485946	chr1:168333963-168333964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183765475	chr1:168333973-168333974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146850000	chr1:168334010-168334011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168329400-168333200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:168329400-168333200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr1:168329400-168333800	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr1:168329400-168334600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:168329600-168333600	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr1:168329600-168334000	Enhancers	Primary T cells fromperipheralblood	blood
7	chr1:168330200-168333600	Weak transcription	HepG2	liver
8	chr1:168330800-168333000	Weak transcription	Right Atrium	heart
9	chr1:168331200-168333000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr1:168331200-168341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:168331600-168333000	Enhancers	Primary hematopoietic stem cells	blood
12	chr1:168331600-168333000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:168331800-168333000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr1:168331800-168333200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:168332000-168333000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr1:168332000-168333200	Enhancers	K562	blood
17	chr1:168332200-168332800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr1:168332200-168333400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:168332400-168333800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr1:168332400-168333800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr1:168332400-168334000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr1:168332600-168335200	Weak transcription	Fetal Heart	heart
23	chr1:168333000-168333200	Enhancers	Right Atrium	heart
24	chr1:168333000-168336000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:168333200-168333800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:168333200-168340800	Weak transcription	Right Atrium	heart
27	chr1:168333600-168334000	Enhancers	HepG2	liver
28	chr1:168333600-168335000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr1:168333800-168334000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:168333800-168334800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:168334000-168335000	Weak transcription	HepG2	liver
32	chr1:168334000-168335200	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr1:168334600-168335400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:168334800-168335400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:168334800-168336000	Enhancers	K562	blood
36	chr1:168335000-168335200	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr1:168335000-168335600	Enhancers	Liver	Liver
38	chr1:168335000-168335800	Enhancers	Fetal Intestine Large	intestine
39	chr1:168335000-168337000	Enhancers	HepG2	liver
40	chr1:168335200-168335400	Enhancers	Primary T cells fromperipheralblood	blood
41	chr1:168335200-168335600	Enhancers	Fetal Heart	heart
42	chr1:168335400-168335600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:168335800-168337200	Weak transcription	Fetal Intestine Large	intestine
44	chr1:168336000-168337200	Weak transcription	K562	blood
45	chr1:168336800-168341800	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:168337000-168337200	Active TSS	A549	lung
47	chr1:168337000-168337800	Flanking Active TSS	HepG2	liver
48	chr1:168337000-168338000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:168337000-168338000	Enhancers	HMEC	breast
50	chr1:168337200-168337400	Enhancers	Fetal Intestine Large	intestine

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