Variant report

Variant	esv3416199
Chromosome Location	chr1:152957887-153005113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:550)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:152995674-152995827	K562	blood:	n/a	n/a
2	ATF1	chr1:152973746-152974221	K562	blood:	n/a	n/a
3	ATF1	chr1:152998366-152998452	K562	blood:	n/a	n/a
4	ATF2	chr1:153004515-153004838	GM12878	blood:	n/a	n/a
5	ATF3	chr1:152995645-152995837	K562	blood:	n/a	n/a
6	BHLHE40	chr1:152995583-152995771	K562	blood:	n/a	n/a
7	BHLHE40	chr1:152958619-152958625	K562	blood:	n/a	n/a
8	CEBPB	chr1:152997666-152997772	K562	blood:	n/a	n/a
9	CEBPB	chr1:153003377-153003680	MCF-7	breast:	n/a	n/a
10	CEBPB	chr1:152968953-152969158	HepG2	liver:	n/a	chr1:152969017-152969028
11	CEBPB	chr1:152995529-152995729	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:152995501-152995879	K562	blood:	n/a	n/a
13	CEBPB	chr1:152992746-152992821	A549	lung:	n/a	n/a
14	CEBPB	chr1:152968999-152969381	H1-hESC	embryonic stem cell:	n/a	chr1:152969017-152969028
15	CHD2	chr1:152965656-152965660	K562	blood:	n/a	n/a
16	CTCF	chr1:152985380-152985530	GM12869	blood:	n/a	n/a
17	CTCF	chr1:153005055-153005092	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:153003360-153003510	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:152991620-152991770	Caco-2	colon:	n/a	n/a
20	CTCF	chr1:152972080-152972230	GM12872	blood:	n/a	n/a
21	E2F4	chr1:152983070-152983284	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr1:152994821-152995147	GM12878	blood:	n/a	n/a
23	EBF1	chr1:152994816-152995065	GM12878	blood:	n/a	n/a
24	ELF1	chr1:152996556-152996811	K562	blood:	n/a	chr1:152996696-152996709
25	EP300	chr1:152995593-152995867	K562	blood:	n/a	n/a
26	EP300	chr1:152995088-152995220	K562	blood:	n/a	n/a
27	FAM48A	chr1:152963200-152963370	GM12878	blood:	n/a	n/a
28	FAM48A	chr1:152983000-152983339	GM12878	blood:	n/a	n/a
29	FAM48A	chr1:152986713-152986884	GM12878	blood:	n/a	n/a
30	FOS	chr1:152998346-152998508	MCF10A-Er-Src	breast:	n/a	chr1:152998406-152998415
31	FOS	chr1:153003332-153003746	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:152959895-152960074	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:153003374-153003737	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:152972902-152973124	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:152973015-152973025	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:152998394-152998560	MCF10A-Er-Src	breast:	n/a	chr1:152998406-152998415
37	FOS	chr1:152972965-152973124	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:152972249-152972421	MCF10A-Er-Src	breast:	n/a	chr1:152972284-152972291 chr1:152972282-152972294 chr1:152972283-152972292 chr1:152972284-152972293 chr1:152972283-152972293
39	FOS	chr1:153003347-153003792	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:152972901-152973072	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:153003381-153003760	MCF10A-Er-Src	breast:	n/a	n/a
42	GATA2	chr1:152993726-152994014	K562	blood:	n/a	n/a
43	GATA3	chr1:152970216-152970812	MCF-7	breast:	n/a	n/a
44	GATA3	chr1:152970276-152970818	T-47D	breast:	n/a	n/a
45	GATA3	chr1:152973850-152974245	T-47D	breast:	n/a	n/a
46	GATA3	chr1:152970932-152971481	MCF-7	breast:	n/a	chr1:152971189-152971197 chr1:152971013-152971020 chr1:152971428-152971444
47	GATA3	chr1:152973753-152974269	MCF-7	breast:	n/a	n/a
48	JUN	chr1:152973884-152974172	K562	blood:	n/a	chr1:152974054-152974062 chr1:152974127-152974141 chr1:152974069-152974078 chr1:152974050-152974061 chr1:152974052-152974064
49	JUN	chr1:152973737-152974252	K562	blood:	n/a	chr1:152974054-152974062 chr1:152974127-152974141 chr1:152974069-152974078 chr1:152974050-152974061 chr1:152974052-152974064
50	JUND	chr1:152973846-152974262	K562	blood:	n/a	chr1:152974054-152974062 chr1:152974127-152974141 chr1:152974069-152974078 chr1:152974050-152974061 chr1:152974052-152974064

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152973720-152973770	AG04449	skin:	fetal
2	chr1:152973720-152973770	AG04449	skin:	fetal
3	chr1:152958102-152958152	NHBE	bronchial:	n/a
4	chr1:152958102-152958152	PANC-1	pancreas:	n/a
5	chr1:152958102-152958152	HAEpiC	amniotic membrane:	n/a
6	chr1:153002762-153002812	HUVEC	blood vessel:	n/a
7	chr1:153002762-153002812	U87	brain:	n/a
8	chr1:152973720-152973770	PrEC	prostate:	n/a
9	chr1:153003198-153003248	HRCEpiC	kidney:	n/a
10	chr1:153003198-153003248	AG04449	skin:	fetal
11	chr1:152973720-152973770	HCPEpiC	choroid plexus:	n/a
12	chr1:152974279-152974329	HUVEC	blood vessel:	n/a
13	chr1:152974771-152974821	Hepatocyte	liver:	n/a
14	chr1:152974771-152974821	HRE	kidney:	n/a
15	chr1:152974771-152974821	HRPEpiC	eye:	n/a
16	chr1:153002762-153002812	RPTEC	kidney:	n/a
17	chr1:152973720-152973770	HCM	heart:	n/a
18	chr1:152973849-152973899	AG10803	skin:	n/a
19	chr1:153003198-153003248	HAEpiC	amniotic membrane:	n/a
20	chr1:152976275-152976325	PANC-1	pancreas:	n/a
21	chr1:152958102-152958152	HRPEpiC	eye:	n/a
22	chr1:152974279-152974329	PrEC	prostate:	n/a
23	chr1:153003198-153003248	Jurkat	blood:	n/a
24	chr1:152973957-152974007	HUVEC	blood vessel:	n/a
25	chr1:152958102-152958152	NT2-D1	testis:	n/a
26	chr1:152973849-152973899	NHBE	bronchial:	n/a
27	chr1:152974771-152974821	HEEpiC	esophagus:	n/a
28	chr1:152976275-152976325	U87	brain:	n/a
29	chr1:152973849-152973899	IMR90	lung:	fetal
30	chr1:152958102-152958152	AoSMC	blood vessel:	n/a
31	chr1:152974279-152974329	HCPEpiC	choroid plexus:	n/a
32	chr1:153003198-153003248	SKMC	muscle:	n/a
33	chr1:153003198-153003248	GM12891	blood:	n/a
34	chr1:152973720-152973770	NHDF-neo	bronchial:	n/a
35	chr1:152974279-152974329	CMK	blood:	n/a
36	chr1:152976275-152976325	HRPEpiC	eye:	n/a
37	chr1:152973957-152974007	HAEpiC	amniotic membrane:	n/a
38	chr1:152974771-152974821	NB4	blood:	n/a
39	chr1:153002762-153002812	ProgFib	skin:	n/a
40	chr1:152974771-152974821	HepG2	liver:	n/a
41	chr1:152958102-152958152	BE2_C	brain:	n/a
42	chr1:153003198-153003248	A549	lung:	n/a
43	chr1:153002762-153002812	ovcar-3	ovarian:	n/a
44	chr1:152973957-152974007	NT2-D1	testis:	n/a
45	chr1:152974771-152974821	U87	brain:	n/a
46	chr1:153002762-153002812	MCF-7	breast:	n/a
47	chr1:152973957-152974007	GM12891	blood:	n/a
48	chr1:152974279-152974329	HNPCEpiC	eye:	n/a
49	chr1:152974279-152974329	BJ	skin:	n/a
50	chr1:152973849-152973899	GM12891	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152999178..153000779-chr1:153005146..153007947,2	MCF-7	breast:
2	chr1:152850201..152851155-chr1:153005077..153005710,4	MCF-7	breast:
3	chr1:152890404..152890921-chr1:153005056..153005990,2	MCF-7	breast:
4	chr1:152988194..152990782-chr20:4228361..4231088,2	MCF-7	breast:
5	chr1:152843289..152844260-chr1:153005064..153006050,2	MCF-7	breast:
6	chr1:152950038..152951690-chr1:152969317..152971115,2	MCF-7	breast:
7	chr1:152975139..152976833-chr1:152995006..152997182,2	MCF-7	breast:
8	chr1:152997979..153000273-chr1:153001489..153003586,2	MCF-7	breast:
9	chr1:152997979..153000273-chr1:153001489..153003586,2	MCF-7	breast:
10	chr1:152975139..152976833-chr1:152995006..152997182,2	MCF-7	breast:
11	chr1:152997652..153000617-chr1:153004018..153006664,2	MCF-7	breast:
12	chr1:152926650..152927561-chr1:153005080..153005744,2	MCF-7	breast:
13	chr1:152962665..152965566-chr1:152972218..152974947,2	K562	blood:
14	chr1:152994189..152995885-chr1:153004714..153007104,2	MCF-7	breast:
15	chr1:152932933..152933748-chr1:153005112..153006074,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRR1A-1	chr1:152957973-152958289	NONHSAT006501
2	lnc-SPRR1A-2	chr1:152974422-152974876	NONHSAT006502
3	lnc-SPRR1B-1	chr1:152996438-152996736	NONHSAT006503
4	lnc-SPRR1A-2	chr1:152974225-152974269	NONHSAT006502

No data

Variant related genes	Relation type
ENSG00000234262	TF binding region
SPRR1B	TF binding region
ENSG00000252920	TF binding region
SPRR3	TF binding region
ENSG00000234262	CpG island
SPRR1B	CpG island
ENSG00000252920	CpG island
SPRR3	CpG island
ENSG00000163209	chromatin interactions
ENSG00000171873	chromatin interactions
ENSG00000169469	chromatin interactions
ENSG00000234262	chromatin interactions
ENSG00000163206	chromatin interactions

Extended variants
information (count: 2220 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2220 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1611764	chr1:152957887-152957888	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199524880	chr1:152957896-152957897	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs79350628	chr1:152957898-152957899	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544987331	chr1:152957900-152957901	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs75299640	chr1:152957904-152957905	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs151244576	chr1:152957933-152957934	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs142988555	chr1:152957934-152957935	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs34727318	chr1:152957944-152957945	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs527509026	chr1:152957955-152957956	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201772388	chr1:152957979-152957980	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs147446158	chr1:152957992-152957993	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs200915905	chr1:152958005-152958006	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs377001066	chr1:152958015-152958016	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs1611765	chr1:152958019-152958020	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs370341601	chr1:152958023-152958024	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs1611766	chr1:152958045-152958046	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531222877	chr1:152958066-152958067	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs569570961	chr1:152958123-152958124	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs1611767	chr1:152958133-152958134	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558517616	chr1:152958146-152958147	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs191892009	chr1:152958153-152958154	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs534435602	chr1:152958158-152958159	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs1611768	chr1:152958165-152958166	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs1611769	chr1:152958166-152958167	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs542779539	chr1:152958177-152958178	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs567767776	chr1:152958198-152958199	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs142859477	chr1:152958213-152958214	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs545264313	chr1:152958219-152958220	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs564882101	chr1:152958230-152958231	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs1129654	chr1:152958238-152958239	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1129655	chr1:152958267-152958268	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs150775699	chr1:152958292-152958293	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs139138503	chr1:152958300-152958301	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs17884726	chr1:152958320-152958321	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs149911922	chr1:152958340-152958341	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571394101	chr1:152958358-152958359	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532058182	chr1:152958373-152958374	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538676411	chr1:152958387-152958388	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs369040942	chr1:152958398-152958399	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs144945050	chr1:152958416-152958417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17880857	chr1:152958485-152958486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17881511	chr1:152958487-152958488	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs17879439	chr1:152958530-152958531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1984198	chr1:152958584-152958585	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554089217	chr1:152958603-152958604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536731536	chr1:152958629-152958630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182029225	chr1:152958636-152958637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148622748	chr1:152958659-152958660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143176417	chr1:152958682-152958683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17886275	chr1:152958723-152958724	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:121)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	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
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
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
Breast cancer	21611746	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
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	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
Follicular lymphoma	18703704	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
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152954200-152966200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:152954400-152969200	Weak transcription	Pancreas	Pancrea
3	chr1:152956800-152965600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:152956800-152972200	Weak transcription	HMEC	breast
5	chr1:152957200-152958400	Active TSS	Esophagus	oesophagus
6	chr1:152965400-152965800	Enhancers	Fetal Brain Male	brain
7	chr1:152965600-152966000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:152965800-152969200	Weak transcription	Fetal Brain Male	brain
9	chr1:152966000-152972200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:152968800-152969800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr1:152969000-152969200	Enhancers	Brain Anterior Caudate	brain
12	chr1:152969000-152969200	Enhancers	Brain Hippocampus Middle	brain
13	chr1:152969000-152969200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:152969000-152969200	Enhancers	Brain Substantia Nigra	brain
15	chr1:152969000-152969400	Enhancers	Esophagus	oesophagus
16	chr1:152969000-152969600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:152969000-152969600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:152969000-152969600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:152969000-152969600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:152969000-152970000	Enhancers	Brain Angular Gyrus	brain
21	chr1:152969000-152970600	Enhancers	Ovary	ovary
22	chr1:152969200-152969400	Flanking Active TSS	Brain Substantia Nigra	brain
23	chr1:152969200-152969600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr1:152969200-152969600	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr1:152969200-152969600	Enhancers	Pancreas	Pancrea
26	chr1:152969200-152969800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:152969200-152969800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:152969200-152969800	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr1:152969200-152969800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr1:152969200-152970000	Enhancers	Brain Cingulate Gyrus	brain
31	chr1:152969200-152971000	Enhancers	Fetal Brain Male	brain
32	chr1:152969400-152970200	Enhancers	Brain Substantia Nigra	brain
33	chr1:152969400-152972000	Weak transcription	Esophagus	oesophagus
34	chr1:152969600-152969800	Enhancers	Brain Hippocampus Middle	brain
35	chr1:152969600-152970000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:152969600-152970600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:152969600-152972000	Weak transcription	Pancreas	Pancrea
38	chr1:152969600-152972600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:152969800-152970200	Weak transcription	Brain Hippocampus Middle	brain
40	chr1:152969800-152970600	Enhancers	Brain Anterior Caudate	brain
41	chr1:152969800-152970600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr1:152970200-152970400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:152970200-152970400	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr1:152970200-152970600	Enhancers	Brain Hippocampus Middle	brain
45	chr1:152970400-152970600	Enhancers	Brain Substantia Nigra	brain
46	chr1:152970600-152974800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:152970600-152975600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr1:152972000-152972200	Enhancers	Pancreas	Pancrea
49	chr1:152972000-152972400	Active TSS	Esophagus	oesophagus
50	chr1:152972200-152973200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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