Variant report

Variant	esv3388149
Chromosome Location	chr1:220205606-220233828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:868)
CpG islands
(count:1038)
Chromatin interactive
region (count:33)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:220232558-220233035	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:220219623-220220158	HepG2	liver:	n/a	n/a
3	ATF1	chr1:220219563-220220219	K562	blood:	n/a	n/a
4	ATF2	chr1:220219748-220220341	GM12878	blood:	n/a	n/a
5	ATF2	chr1:220219565-220220272	GM12878	blood:	n/a	n/a
6	ATF2	chr1:220219656-220220278	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:220219600-220220227	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr1:220219554-220220202	K562	blood:	n/a	n/a
9	ATF3	chr1:220219496-220220172	K562	blood:	n/a	n/a
10	ATF3	chr1:220219774-220220156	HepG2	liver:	n/a	n/a
11	ATF3	chr1:220219499-220220214	A549	lung:	n/a	n/a
12	ATF3	chr1:220219641-220220318	GM12878	blood:	n/a	n/a
13	ATF3	chr1:220219813-220220193	GM12878	blood:	n/a	n/a
14	ATF3	chr1:220219549-220220234	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr1:220219641-220220368	HepG2	liver:	n/a	n/a
16	ATF3	chr1:220219646-220220179	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr1:220219432-220220194	K562	blood:	n/a	n/a
18	BACH1	chr1:220219222-220220191	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr1:220219493-220220070	GM12878	blood:	n/a	n/a
20	BCL3	chr1:220219673-220220378	A549	lung:	n/a	n/a
21	BCL3	chr1:220219340-220220300	A549	lung:	n/a	n/a
22	BCLAF1	chr1:220219483-220220273	GM12878	blood:	n/a	n/a
23	BCLAF1	chr1:220219579-220220310	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:220219655-220220061	A549	lung:	n/a	n/a
25	BHLHE40	chr1:220219128-220220274	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:220218606-220218845	K562	blood:	n/a	n/a
27	BHLHE40	chr1:220219279-220220237	K562	blood:	n/a	n/a
28	BRCA1	chr1:220219768-220220112	HepG2	liver:	n/a	n/a
29	BRCA1	chr1:220219673-220220245	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:220219278-220220304	HCT-116	colon:	n/a	n/a
31	CBX3	chr1:220219669-220220260	K562	blood:	n/a	n/a
32	CBX3	chr1:220219336-220220296	K562	blood:	n/a	n/a
33	CCNT2	chr1:220219391-220220101	K562	blood:	n/a	n/a
34	CEBPB	chr1:220219467-220220178	HepG2	liver:	n/a	chr1:220219642-220219659
35	CEBPB	chr1:220219469-220220165	IMR90	lung:	n/a	chr1:220219642-220219659
36	CEBPB	chr1:220219453-220220308	K562	blood:	n/a	chr1:220219642-220219659
37	CEBPB	chr1:220214515-220214723	K562	blood:	n/a	n/a
38	CEBPB	chr1:220226213-220226362	K562	blood:	n/a	n/a
39	CEBPB	chr1:220219506-220220149	HepG2	liver:	n/a	chr1:220219642-220219659
40	CEBPB	chr1:220207669-220207703	A549	lung:	n/a	n/a
41	CEBPB	chr1:220232542-220232888	HepG2	liver:	n/a	chr1:220232709-220232720
42	CEBPB	chr1:220219460-220220186	A549	lung:	n/a	chr1:220219642-220219659
43	CEBPB	chr1:220219403-220220223	Hela-S3	cervix:	n/a	chr1:220219642-220219659
44	CEBPB	chr1:220232569-220232924	HepG2	liver:	n/a	chr1:220232709-220232720
45	CEBPB	chr1:220232543-220232866	HepG2	liver:	n/a	chr1:220232709-220232720
46	CEBPB	chr1:220232584-220232804	HepG2	liver:	n/a	chr1:220232709-220232720
47	CEBPB	chr1:220219458-220220172	K562	blood:	n/a	chr1:220219642-220219659
48	CEBPB	chr1:220219490-220220175	H1-hESC	embryonic stem cell:	n/a	chr1:220219642-220219659
49	CEBPB	chr1:220218024-220218450	K562	blood:	n/a	n/a
50	CEBPD	chr1:220232553-220232749	HepG2	liver:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220219742-220219792	ECC-1	luminal epithelium:	n/a
2	chr1:220219742-220219792	ECC-1	luminal epithelium:	n/a
3	chr1:220220036-220220086	CMK	blood:	n/a
4	chr1:220220103-220220153	K562	blood:	n/a
5	chr1:220216811-220216861	U87	brain:	n/a
6	chr1:220221233-220221283	HNPCEpiC	eye:	n/a
7	chr1:220220060-220220110	HNPCEpiC	eye:	n/a
8	chr1:220216811-220216861	HRE	kidney:	n/a
9	chr1:220219195-220219245	K562	blood:	n/a
10	chr1:220220103-220220153	PFSK-1	brain:	n/a
11	chr1:220219430-220219480	NH-A	brain:	n/a
12	chr1:220219598-220219648	HEEpiC	esophagus:	n/a
13	chr1:220219163-220219213	ovcar-3	ovarian:	n/a
14	chr1:220222487-220222537	HNPCEpiC	eye:	n/a
15	chr1:220222487-220222537	PrEC	prostate:	n/a
16	chr1:220219598-220219648	BJ	skin:	n/a
17	chr1:220219722-220219772	NB4	blood:	n/a
18	chr1:220219722-220219772	HepG2	liver:	n/a
19	chr1:220221233-220221283	NH-A	brain:	n/a
20	chr1:220219823-220219873	NB4	blood:	n/a
21	chr1:220222487-220222537	MCF-7	breast:	n/a
22	chr1:220221233-220221283	Jurkat	blood:	n/a
23	chr1:220219598-220219648	IMR90	lung:	fetal
24	chr1:220219742-220219792	Caco-2	colon:	n/a
25	chr1:220232018-220232068	AG09319	gingival:	n/a
26	chr1:220219906-220219956	ovcar-3	ovarian:	n/a
27	chr1:220220060-220220110	HCT-116	colon:	n/a
28	chr1:220219163-220219213	HIPEpiC	eye:	n/a
29	chr1:220221462-220221512	GM12891	blood:	n/a
30	chr1:220219430-220219480	HEEpiC	esophagus:	n/a
31	chr1:220220103-220220153	HepG2	liver:	n/a
32	chr1:220221233-220221283	HMEC	breast:	n/a
33	chr1:220219430-220219480	HCF	heart:	n/a
34	chr1:220219823-220219873	NH-A	brain:	n/a
35	chr1:220220103-220220153	HMEC	breast:	n/a
36	chr1:220219906-220219956	CMK	blood:	n/a
37	chr1:220219742-220219792	SK-N-MC	brain:	n/a
38	chr1:220216811-220216861	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:220219722-220219772	PFSK-1	brain:	n/a
40	chr1:220219598-220219648	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:220219906-220219956	HCF	heart:	n/a
42	chr1:220220103-220220153	BE2_C	brain:	n/a
43	chr1:220220036-220220086	HEEpiC	esophagus:	n/a
44	chr1:220219823-220219873	Hela-S3	cervix:	n/a
45	chr1:220221233-220221283	K562	blood:	n/a
46	chr1:220219906-220219956	U87	brain:	n/a
47	chr1:220220103-220220153	ovcar-3	ovarian:	n/a
48	chr1:220232018-220232068	GM19239	blood:	n/a
49	chr1:220232018-220232068	Hela-S3	cervix:	n/a
50	chr1:220232018-220232068	LNCaP	prostate:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:220219093..220220220-chr15:66084111..66084775,3	Hela-S3	cervix:
2	chr1:220138957..220140569-chr1:220217050..220219686,2	K562	blood:
3	chr1:220219668..220220272-chr1:247373675..247374229,2	Hela-S3	cervix:
4	chr1:220209718..220212778-chr1:220216575..220219154,4	K562	blood:
5	chr1:220214211..220216766-chr1:220216909..220219452,2	MCF-7	breast:
6	chr1:220217537..220219750-chr1:220295098..220297083,2	K562	blood:
7	chr1:220209718..220212778-chr1:220216575..220219154,4	K562	blood:
8	chr1:220212894..220215277-chr1:220216645..220218222,3	K562	blood:
9	chr1:220215698..220219502-chr1:220266015..220268343,4	K562	blood:
10	chr1:220214211..220216766-chr1:220216909..220219452,2	MCF-7	breast:
11	chr1:220218207..220221672-chr1:220261461..220265020,3	K562	blood:
12	chr1:220219151..220219774-chr19:47852496..47853071,2	NB4	blood:
13	chr1:220198252..220200189-chr1:220204982..220206725,3	K562	blood:
14	chr1:220190580..220193578-chr1:220217938..220219443,2	K562	blood:
15	chr1:220218535..220220494-chr1:220265581..220269628,4	MCF-7	breast:
16	chr1:220219521..220220100-chr1:220262803..220263613,2	K562	blood:
17	chr1:11714821..11715495-chr1:220219634..220220255,2	HCT-116	colon:
18	chr1:220009776..220012687-chr1:220217353..220218943,2	K562	blood:
19	chr1:220204428..220207144-chr1:220209428..220212102,2	MCF-7	breast:
20	chr1:220218765..220221462-chr1:220223593..220225505,2	MCF-7	breast:
21	chr1:220215559..220218002-chr1:220218306..220221270,3	MCF-7	breast:
22	chr1:220212894..220215277-chr1:220216645..220218222,3	K562	blood:
23	chr1:220229568..220231536-chr1:220233409..220234910,2	K562	blood:
24	chr1:220215698..220221065-chr1:220265352..220268996,5	K562	blood:
25	chr1:220219640..220220523-chr5:139493361..139494034,2	Hela-S3	cervix:
26	chr1:220193445..220195107-chr1:220205379..220207887,2	K562	blood:
27	chr1:220218169..220221765-chr1:220261064..220269153,11	MCF-7	breast:
28	chr1:220219736..220221759-chr1:220265959..220267842,3	K562	blood:
29	chr1:220219302..220219842-chr11:64878697..64879528,2	NB4	blood:
30	chr1:220229568..220231536-chr1:220233409..220234910,2	K562	blood:
31	chr1:220196455..220198448-chr1:220208352..220209875,2	K562	blood:
32	chr1:220212014..220214068-chr1:220216759..220219974,3	MCF-7	breast:
33	chr1:220204428..220207144-chr1:220209428..220212102,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IARS2-2	chr1:220206306-220206467	NONHSAT009574
2	lnc-IARS2-2	chr1:220208313-220208461	NONHSAT009574
3	lnc-IARS2-2	chr1:220222965-220223108	NONHSAT009574
4	lnc-EPRS-2	chr1:220231103-220231259	NONHSAT009576
5	lnc-IARS2-2	chr1:220222965-220223108	NONHSAT009575
6	lnc-EPRS-1	chr1:220218325-220218488	NONHSAT009572
7	lnc-IARS2-2	chr1:220224019-220224929	NONHSAT009575
8	lnc-IARS2-2	chr1:220206375-220206467	NONHSAT009575

No data

Variant related genes	Relation type
EPRS	TF binding region
EPRS	CpG island
ENSG00000174485	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000136628	chromatin interactions
ENSG00000132879	chromatin interactions
ENSG00000134815	chromatin interactions
ENSG00000162813	chromatin interactions
ENSG00000227671	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000067704	chromatin interactions

Extended variants
information (count: 1080 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192979584	chr1:220205621-220205622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74572119	chr1:220205627-220205628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541666310	chr1:220205644-220205645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149142917	chr1:220205670-220205671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555716159	chr1:220205671-220205672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572329162	chr1:220205674-220205675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377021548	chr1:220205682-220205683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534604799	chr1:220205689-220205690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199654586	chr1:220205691-220205692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201015628	chr1:220205693-220205694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77524985	chr1:220205694-220205695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77421683	chr1:220205696-220205697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577704073	chr1:220205703-220205704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34457701	chr1:220205704-220205705	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs115489488	chr1:220205705-220205706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548889502	chr1:220205706-220205707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574414616	chr1:220205713-220205714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201466798	chr1:220205714-220205715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371266273	chr1:220205775-220205776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10987	chr1:220205848-220205849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374210879	chr1:220205860-220205861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368115475	chr1:220205894-220205895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562051327	chr1:220205912-220205913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2789816	chr1:220205943-220205944	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547430305	chr1:220205969-220205970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564491988	chr1:220205971-220205972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2577138	chr1:220205980-220205981	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs550271004	chr1:220206015-220206016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570020038	chr1:220206028-220206029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532651611	chr1:220206033-220206034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7531703	chr1:220206035-220206036	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs192460636	chr1:220206062-220206063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566025891	chr1:220206069-220206070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534906973	chr1:220206085-220206086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184744204	chr1:220206122-220206123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577543353	chr1:220206159-220206160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374505354	chr1:220206178-220206179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536612783	chr1:220206186-220206187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557032966	chr1:220206196-220206197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542407240	chr1:220206215-220206216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142330322	chr1:220206245-220206246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151286258	chr1:220206259-220206260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6692978	chr1:220206331-220206332	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570760829	chr1:220206387-220206388	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs111644577	chr1:220206390-220206391	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs370344804	chr1:220206412-220206413	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs116141600	chr1:220206436-220206437	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs75703586	chr1:220206465-220206466	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs564598307	chr1:220206475-220206476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533378878	chr1:220206565-220206566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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	21858162	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220166200-220208400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:220166200-220209000	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr1:220166400-220206800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:220166400-220210600	Strong transcription	Duodenum Mucosa	Duodenum
5	chr1:220166800-220208400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:220167800-220211800	Weak transcription	Stomach Mucosa	stomach
7	chr1:220168400-220213800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:220169200-220206400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:220170400-220218600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:220172600-220218600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:220176000-220208000	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:220176400-220208400	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:220177600-220205800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr1:220178000-220217800	Weak transcription	Pancreas	Pancrea
15	chr1:220178200-220218600	Weak transcription	Right Ventricle	heart
16	chr1:220186600-220207800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:220187200-220216800	Weak transcription	Fetal Heart	heart
18	chr1:220187400-220216800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:220189200-220208000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:220189600-220208400	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr1:220190800-220208400	Strong transcription	Liver	Liver
22	chr1:220190800-220210400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:220192600-220206800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:220193600-220218600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:220194800-220206800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:220194800-220211600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:220194800-220211800	Weak transcription	Esophagus	oesophagus
28	chr1:220194800-220212200	Weak transcription	Aorta	Aorta
29	chr1:220196400-220211600	Weak transcription	Gastric	stomach
30	chr1:220196400-220218200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr1:220196600-220212200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr1:220197200-220217800	Weak transcription	Colonic Mucosa	Colon
33	chr1:220197400-220212000	Weak transcription	Small Intestine	intestine
34	chr1:220197600-220211800	Weak transcription	Spleen	Spleen
35	chr1:220197800-220205800	Weak transcription	Brain Germinal Matrix	brain
36	chr1:220197800-220205800	Weak transcription	Psoas Muscle	Psoas
37	chr1:220198200-220206000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:220199600-220216800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:220200200-220212200	Strong transcription	GM12878-XiMat	blood
40	chr1:220200800-220208000	Strong transcription	Adipose Nuclei	Adipose
41	chr1:220200800-220210200	Strong transcription	Dnd41	blood
42	chr1:220201000-220206800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:220201000-220208000	Strong transcription	Osteobl	bone
44	chr1:220201000-220208800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:220201000-220209200	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr1:220201200-220208200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:220201200-220208600	Strong transcription	Primary B cells from peripheral blood	blood
48	chr1:220201400-220208000	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr1:220201400-220208200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:220201400-220208200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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