Variant report

Variant	esv3419617
Chromosome Location	chr1:155198528-155202826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:184)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:155201138-155201473	K562	blood:	n/a	n/a
2	CEBPB	chr1:155200733-155201030	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:155200775-155200957	K562	blood:	n/a	n/a
4	CEBPB	chr1:155200679-155201037	Hela-S3	cervix:	n/a	n/a
5	GABPA	chr1:155202649-155203018	Hela-S3	cervix:	n/a	n/a
6	GABPA	chr1:155202786-155202938	HepG2	liver:	n/a	n/a
7	GABPA	chr1:155202753-155202956	HepG2	liver:	n/a	n/a
8	HEY1	chr1:155202769-155203044	K562	blood:	n/a	n/a
9	MAFK	chr1:155200361-155200585	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr1:155201432-155201459	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr1:155202687-155202711	GM12878	blood:	n/a	n/a
12	POLR2A	chr1:155201541-155201575	HepG2	liver:	n/a	n/a
13	POLR2A	chr1:155200757-155201471	K562	blood:	n/a	n/a
14	POLR2A	chr1:155201040-155201258	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr1:155202574-155202968	GM12878	blood:	n/a	n/a
16	POLR2A	chr1:155201025-155201042	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr1:155202541-155203064	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:155202042-155202050	K562	blood:	n/a	n/a
19	POLR2A	chr1:155201108-155201119	MCF-7	breast:	n/a	n/a
20	POLR2A	chr1:155201581-155201693	HepG2	liver:	n/a	n/a
21	POLR2A	chr1:155201697-155202160	SK-N-MC	brain:	n/a	n/a
22	POLR2A	chr1:155202732-155202958	MCF-7	breast:	n/a	n/a
23	POLR2A	chr1:155202069-155202118	K562	blood:	n/a	n/a
24	POLR2A	chr1:155202593-155203996	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr1:155202394-155202760	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr1:155199455-155199497	HepG2	liver:	n/a	n/a
27	POLR2A	chr1:155202369-155202566	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr1:155202300-155204022	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr1:155201949-155203088	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr1:155201839-155202585	GM12892	blood:	n/a	n/a
31	POLR2A	chr1:155201244-155201382	MCF-7	breast:	n/a	n/a
32	POLR2A	chr1:155201081-155201368	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr1:155202040-155202537	GM12878	blood:	n/a	n/a
34	POLR2A	chr1:155198841-155198850	GM12878	blood:	n/a	n/a
35	POLR2A	chr1:155201056-155201467	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr1:155202579-155203237	HepG2	liver:	n/a	n/a
37	POLR2A	chr1:155201173-155201649	ProgFib	skin:	n/a	n/a
38	POLR2A	chr1:155201734-155202094	HepG2	liver:	n/a	n/a
39	POLR2A	chr1:155200708-155200834	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr1:155202473-155202669	ProgFib	skin:	n/a	n/a
41	POLR2A	chr1:155200880-155200900	ProgFib	skin:	n/a	n/a
42	POLR2A	chr1:155200981-155201375	U87	brain:	n/a	n/a
43	POLR2A	chr1:155198633-155198715	GM12878	blood:	n/a	n/a
44	POLR2A	chr1:155201223-155201226	MCF-7	breast:	n/a	n/a
45	POLR2A	chr1:155202783-155202922	K562	blood:	n/a	n/a
46	POLR2A	chr1:155202154-155202488	HepG2	liver:	n/a	n/a
47	POLR2A	chr1:155201484-155201501	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr1:155202044-155204350	PFSK-1	brain:	n/a	n/a
49	POLR2A	chr1:155201045-155201593	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr1:155202727-155203107	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155202685-155202735	Caco-2	colon:	n/a
2	chr1:155202685-155202735	Caco-2	colon:	n/a
3	chr1:155202674-155202724	A549	lung:	n/a
4	chr1:155202685-155202735	BJ	skin:	n/a
5	chr1:155202685-155202735	ECC-1	luminal epithelium:	n/a
6	chr1:155202685-155202735	NB4	blood:	n/a
7	chr1:155202674-155202724	AG09319	gingival:	n/a
8	chr1:155200357-155200407	SK-N-SH	brain:	n/a
9	chr1:155200357-155200407	SK-N-SH_RA	brain:	n/a
10	chr1:155200357-155200407	Hepatocyte	liver:	n/a
11	chr1:155202685-155202735	SAEC	small airway:	n/a
12	chr1:155202674-155202724	NT2-D1	testis:	n/a
13	chr1:155202685-155202735	HUVEC	blood vessel:	n/a
14	chr1:155202674-155202724	SK-N-SH_RA	brain:	n/a
15	chr1:155202685-155202735	AoSMC	blood vessel:	n/a
16	chr1:155202674-155202724	HCF	heart:	n/a
17	chr1:155202685-155202735	HRE	kidney:	n/a
18	chr1:155200357-155200407	PrEC	prostate:	n/a
19	chr1:155202685-155202735	GM12878	blood:	n/a
20	chr1:155202685-155202735	SKMC	muscle:	n/a
21	chr1:155200357-155200407	HIPEpiC	eye:	n/a
22	chr1:155202674-155202724	GM12891	blood:	n/a
23	chr1:155200357-155200407	ovcar-3	ovarian:	n/a
24	chr1:155202674-155202724	SK-N-MC	brain:	n/a
25	chr1:155202674-155202724	ProgFib	skin:	n/a
26	chr1:155200357-155200407	AG04450	lung:	fetal
27	chr1:155202674-155202724	SK-N-SH	brain:	n/a
28	chr1:155202685-155202735	HCT-116	colon:	n/a
29	chr1:155200357-155200407	HAEpiC	amniotic membrane:	n/a
30	chr1:155202685-155202735	NT2-D1	testis:	n/a
31	chr1:155202685-155202735	ProgFib	skin:	n/a
32	chr1:155202674-155202724	U87	brain:	n/a
33	chr1:155200357-155200407	HUVEC	blood vessel:	n/a
34	chr1:155202685-155202735	LNCaP	prostate:	n/a
35	chr1:155202674-155202724	HAEpiC	amniotic membrane:	n/a
36	chr1:155200357-155200407	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:155202685-155202735	Hela-S3	cervix:	n/a
38	chr1:155202685-155202735	HNPCEpiC	eye:	n/a
39	chr1:155202685-155202735	HL-60	blood:	n/a
40	chr1:155202674-155202724	Jurkat	blood:	n/a
41	chr1:155202674-155202724	NHDF-neo	bronchial:	n/a
42	chr1:155200357-155200407	PANC-1	pancreas:	n/a
43	chr1:155202685-155202735	GM12892	blood:	n/a
44	chr1:155200357-155200407	AG09319	gingival:	n/a
45	chr1:155202674-155202724	GM06990	blood:	n/a
46	chr1:155202685-155202735	MCF-7	breast:	n/a
47	chr1:155202685-155202735	HCM	heart:	n/a
48	chr1:155200357-155200407	ProgFib	skin:	n/a
49	chr1:155200357-155200407	HRCEpiC	kidney:	n/a
50	chr1:155200357-155200407	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:155195599..155199380-chr1:155211353..155216703,7	MCF-7	breast:
2	chr1:155054721..155059011-chr1:155196588..155199418,3	K562	blood:
3	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
4	chr1:155187581..155189617-chr1:155195998..155199387,4	MCF-7	breast:
5	chr1:155143901..155153030-chr1:155191166..155199183,23	MCF-7	breast:
6	chr1:155200126..155202062-chr1:155213409..155215894,2	MCF-7	breast:
7	chr1:155169616..155173195-chr1:155194780..155198735,4	MCF-7	breast:
8	chr1:155196791..155199483-chr1:155201481..155203519,3	K562	blood:
9	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
10	chr1:155172877..155174474-chr1:155197003..155199061,2	K562	blood:
11	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
12	chr1:155174590..155181850-chr1:155192419..155201858,28	K562	blood:
13	chr1:155187302..155192095-chr1:155195846..155198767,7	MCF-7	breast:
14	chr1:155174605..155182734-chr1:155187211..155200915,43	MCF-7	breast:
15	chr1:155171519..155180465-chr1:155194608..155199196,19	MCF-7	breast:
16	chr1:155197587..155199547-chr1:155278190..155280905,2	MCF-7	breast:
17	chr1:155195512..155198962-chr1:155200125..155202735,3	MCF-7	breast:
18	chr1:155195512..155198962-chr1:155200125..155202735,3	MCF-7	breast:
19	chr1:155098008..155101008-chr1:155194682..155198746,4	MCF-7	breast:
20	chr1:155144282..155146428-chr1:155196994..155199261,3	K562	blood:
21	chr1:155196524..155199471-chr1:155205933..155208728,2	MCF-7	breast:
22	chr1:155200769..155203124-chr1:155222632..155225230,2	K562	blood:
23	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
24	chr1:155098847..155100942-chr1:155197257..155198807,2	K562	blood:
25	chr1:155196978..155198560-chr1:155209319..155211586,2	K562	blood:
26	chr1:155195406..155199356-chr1:155210414..155216260,10	K562	blood:
27	chr1:155200890..155203810-chr1:155211180..155212788,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GBA-1	chr1:155201063-155203428	NONHSAT006710

No data

Variant related genes	Relation type
MTX1P1	TF binding region
GBAP1	TF binding region
MTX1P1	CpG island
GBAP1	CpG island
ENSG00000160767	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000236675	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000273088	chromatin interactions

Extended variants
information (count: 149 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:149 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561136364	chr1:155198579-155198580	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs573104679	chr1:155198590-155198591	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs376082977	chr1:155198638-155198639	Weak transcription Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs555375706	chr1:155198642-155198643	Weak transcription Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs139030264	chr1:155198758-155198759	Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs565279757	chr1:155198762-155198763	Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
7	rs112270735	chr1:155198771-155198772	Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	mRNA abundance
8	rs184392878	chr1:155198822-155198823	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs562911722	chr1:155198887-155198888	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs570155070	chr1:155198892-155198893	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs377501757	chr1:155198893-155198894	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs115650169	chr1:155198904-155198905	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs114090048	chr1:155198910-155198911	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs557936468	chr1:155198925-155198926	Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs566807167	chr1:155198967-155198968	Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs376393333	chr1:155199053-155199054	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs370011489	chr1:155199061-155199062	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs570909213	chr1:155199062-155199063	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs538733055	chr1:155199071-155199072	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs189660667	chr1:155199092-155199093	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs535922581	chr1:155199156-155199157	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs150915663	chr1:155199210-155199211	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs181495640	chr1:155199308-155199309	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs12407919	chr1:155199315-155199316	Weak transcription	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs186289485	chr1:155199356-155199357	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs573168996	chr1:155199420-155199421	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs540105087	chr1:155199520-155199521	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs11264343	chr1:155199666-155199667	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs149891553	chr1:155199674-155199675	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs35314978	chr1:155199691-155199692	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs558577796	chr1:155199751-155199752	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs562814456	chr1:155199760-155199761	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs562655127	chr1:155199761-155199762	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs530068938	chr1:155199774-155199775	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs548167854	chr1:155199779-155199780	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs560496384	chr1:155199787-155199788	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs559287855	chr1:155199816-155199817	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs189617710	chr1:155199817-155199818	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs528593621	chr1:155199898-155199899	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs527982312	chr1:155199922-155199923	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs552551780	chr1:155199934-155199935	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs571038289	chr1:155199940-155199941	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs531781468	chr1:155199946-155199947	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550677841	chr1:155199952-155199953	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568959220	chr1:155199961-155199962	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536295173	chr1:155199983-155199984	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs554604124	chr1:155200013-155200014	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs180841705	chr1:155200020-155200021	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs186262913	chr1:155200097-155200098	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs552747204	chr1:155200172-155200173	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	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
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155197000-155205800	Weak transcription	Gastric	stomach
2	chr1:155197200-155212800	Weak transcription	Small Intestine	intestine
3	chr1:155198000-155200400	Weak transcription	HepG2	liver
4	chr1:155198000-155201000	Weak transcription	NH-A	brain
5	chr1:155198000-155201200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:155198000-155201400	Weak transcription	Osteobl	bone
7	chr1:155198000-155201600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:155198000-155201800	Weak transcription	Ovary	ovary
9	chr1:155198000-155201800	Weak transcription	HUVEC	blood vessel
10	chr1:155198000-155202000	Weak transcription	Aorta	Aorta
11	chr1:155198000-155202000	Weak transcription	Pancreas	Pancrea
12	chr1:155198000-155202000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:155198000-155204600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:155198000-155204800	Weak transcription	Esophagus	oesophagus
15	chr1:155198000-155205000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:155198000-155205000	Weak transcription	Liver	Liver
17	chr1:155198000-155205000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr1:155198000-155205000	Weak transcription	Thymus	Thymus
19	chr1:155198000-155205400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:155198000-155205400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr1:155198000-155205600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:155198000-155205600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:155198000-155205800	Weak transcription	Primary B cells from cord blood	blood
24	chr1:155198000-155205800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr1:155198000-155206800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:155198000-155209600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr1:155198000-155210400	Weak transcription	A549	lung
28	chr1:155198000-155210400	Weak transcription	HMEC	breast
29	chr1:155198000-155210400	Weak transcription	HSMM	muscle
30	chr1:155198000-155210600	Weak transcription	Psoas Muscle	Psoas
31	chr1:155198000-155210800	Weak transcription	Fetal Kidney	kidney
32	chr1:155198200-155198600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:155198200-155198600	Enhancers	Brain Germinal Matrix	brain
34	chr1:155198200-155198600	Enhancers	Dnd41	blood
35	chr1:155198200-155198800	Enhancers	K562	blood
36	chr1:155198200-155201000	Weak transcription	Rectal Smooth Muscle	rectum
37	chr1:155198200-155201200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:155198200-155201200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:155198200-155201200	Weak transcription	Fetal Muscle Trunk	muscle
40	chr1:155198200-155201800	Weak transcription	Fetal Lung	lung
41	chr1:155198200-155201800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr1:155198200-155201800	Weak transcription	HSMMtube	muscle
43	chr1:155198200-155202000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:155198200-155202000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:155198200-155202000	Weak transcription	Brain Anterior Caudate	brain
46	chr1:155198200-155202000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr1:155198200-155202200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:155198200-155202400	Weak transcription	Spleen	Spleen
49	chr1:155198200-155202600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:155198200-155204600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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