Variant report

Variant	esv3402740
Chromosome Location	chr1:95500980-95527860
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	ARID3A	chr1:95508972-95509298	K562	blood:	n/a	n/a
2	ARID3A	chr1:95508891-95509268	HepG2	liver:	n/a	n/a
3	ATF1	chr1:95508991-95509289	K562	blood:	n/a	n/a
4	ATF3	chr1:95508953-95509280	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:95525742-95525744	K562	blood:	n/a	n/a
6	BACH1	chr1:95509013-95509438	K562	blood:	n/a	n/a
7	BHLHE40	chr1:95508997-95509297	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:95508992-95509291	K562	blood:	n/a	n/a
9	BRCA1	chr1:95508986-95509273	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr1:95508993-95509322	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:95500993-95501648	HCT-116	colon:	n/a	chr1:95501517-95501530
12	CEBPB	chr1:95501055-95501625	IMR90	lung:	n/a	chr1:95501517-95501530
13	CEBPB	chr1:95501056-95501613	HCT-116	colon:	n/a	chr1:95501517-95501530
14	CEBPB	chr1:95508998-95509247	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr1:95527100-95527399	K562	blood:	n/a	n/a
16	CHD1	chr1:95508719-95509501	IMR90	lung:	n/a	n/a
17	CHD2	chr1:95508967-95509328	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:95509003-95509270	K562	blood:	n/a	n/a
19	CHD2	chr1:95504900-95505001	HepG2	liver:	n/a	n/a
20	CHD2	chr1:95508991-95509307	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr1:95509012-95509222	A549	lung:	n/a	n/a
22	CTCF	chr1:95509080-95509230	NB4	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
23	CTCF	chr1:95508839-95509381	H1-hESC	embryonic stem cell:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
24	CTCF	chr1:95507188-95507462	Kidney_OC	kidney:	n/a	chr1:95507330-95507346
25	CTCF	chr1:95507200-95507350	HRE	kidney:	n/a	chr1:95507330-95507346
26	CTCF	chr1:95508990-95509286	Fibrobl	skin:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
27	CTCF	chr1:95507240-95507390	BE2_C	brain:	n/a	chr1:95507330-95507346
28	CTCF	chr1:95507240-95507390	HL-60	blood:	n/a	chr1:95507330-95507346
29	CTCF	chr1:95509040-95509190	HepG2	liver:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
30	CTCF	chr1:95507119-95507407	A549	lung:	n/a	chr1:95507330-95507346
31	CTCF	chr1:95509060-95509210	GM12878	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
32	CTCF	chr1:95509060-95509210	AG04449	skin:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
33	CTCF	chr1:95508693-95509369	IMR90	lung:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
34	CTCF	chr1:95507212-95507393	GM19240	blood:	n/a	chr1:95507330-95507346
35	CTCF	chr1:95508992-95509285	LNCaP	prostate:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
36	CTCF	chr1:95507240-95507390	HEEpiC	esophagus:	n/a	chr1:95507330-95507346
37	CTCF	chr1:95507200-95507350	HEK293	kidney:	n/a	chr1:95507330-95507346
38	CTCF	chr1:95507240-95507390	HFF-Myc	foreskin:	n/a	chr1:95507330-95507346
39	CTCF	chr1:95526625-95526740	K562	blood:	n/a	n/a
40	CTCF	chr1:95508777-95509465	GM12878	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
41	CTCF	chr1:95507220-95507370	BJ	skin:	n/a	chr1:95507330-95507346
42	CTCF	chr1:95507820-95507970	K562	blood:	n/a	n/a
43	CTCF	chr1:95509080-95509230	GM12878	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
44	CTCF	chr1:95509060-95509210	GM12875	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
45	CTCF	chr1:95509040-95509190	AG09309	skin:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
46	CTCF	chr1:95509040-95509190	GM12873	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
47	CTCF	chr1:95508829-95509430	K562	blood:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
48	CTCF	chr1:95507260-95507410	RPTEC	kidney:	n/a	chr1:95507330-95507346
49	CTCF	chr1:95508983-95509308	Pancreas_OC	pancreas:	n/a	chr1:95509148-95509166 chr1:95509151-95509161 chr1:95509154-95509163 chr1:95509150-95509163 chr1:95509149-95509165 chr1:95509143-95509164 chr1:95509153-95509166 chr1:95509150-95509168
50	CTCF	chr1:95509380-95509530	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95509099-95509149	HNPCEpiC	eye:	n/a
2	chr1:95508854-95508904	HCM	heart:	n/a
3	chr1:95508854-95508904	HCPEpiC	choroid plexus:	n/a
4	chr1:95508854-95508904	HMEC	breast:	n/a
5	chr1:95509099-95509149	SAEC	small airway:	n/a
6	chr1:95509099-95509149	NB4	blood:	n/a
7	chr1:95509099-95509149	HCF	heart:	n/a
8	chr1:95508854-95508904	HIPEpiC	eye:	n/a
9	chr1:95508854-95508904	A549	lung:	n/a
10	chr1:95509099-95509149	MCF10A-Er-Src	breast:	n/a
11	chr1:95509099-95509149	CMK	blood:	n/a
12	chr1:95508854-95508904	K562	blood:	n/a
13	chr1:95509099-95509149	ovcar-3	ovarian:	n/a
14	chr1:95508854-95508904	NH-A	brain:	n/a
15	chr1:95509099-95509149	LNCaP	prostate:	n/a
16	chr1:95509099-95509149	PrEC	prostate:	n/a
17	chr1:95509099-95509149	HEK293	kidney:	embryo
18	chr1:95508854-95508904	SK-N-SH	brain:	n/a
19	chr1:95508854-95508904	RPTEC	kidney:	n/a
20	chr1:95508854-95508904	HEK293	kidney:	embryo
21	chr1:95509099-95509149	ProgFib	skin:	n/a
22	chr1:95508854-95508904	BE2_C	brain:	n/a
23	chr1:95509099-95509149	GM12891	blood:	n/a
24	chr1:95509099-95509149	HCT-116	colon:	n/a
25	chr1:95509099-95509149	AG04449	skin:	fetal
26	chr1:95509099-95509149	NHDF-neo	bronchial:	n/a
27	chr1:95508854-95508904	SK-N-SH_RA	brain:	n/a
28	chr1:95508854-95508904	HAEpiC	amniotic membrane:	n/a
29	chr1:95509099-95509149	SKMC	muscle:	n/a
30	chr1:95508854-95508904	ProgFib	skin:	n/a
31	chr1:95508854-95508904	MCF-7	breast:	n/a
32	chr1:95509099-95509149	BJ	skin:	n/a
33	chr1:95508854-95508904	U87	brain:	n/a
34	chr1:95509099-95509149	BE2_C	brain:	n/a
35	chr1:95509099-95509149	AG10803	skin:	n/a
36	chr1:95509099-95509149	GM06990	blood:	n/a
37	chr1:95509099-95509149	Hela-S3	cervix:	n/a
38	chr1:95508854-95508904	HUVEC	blood vessel:	n/a
39	chr1:95508854-95508904	NHDF-neo	bronchial:	n/a
40	chr1:95508854-95508904	HCF	heart:	n/a
41	chr1:95509099-95509149	PFSK-1	brain:	n/a
42	chr1:95508854-95508904	CMK	blood:	n/a
43	chr1:95508854-95508904	SK-N-MC	brain:	n/a
44	chr1:95508854-95508904	HRPEpiC	eye:	n/a
45	chr1:95508854-95508904	ovcar-3	ovarian:	n/a
46	chr1:95509099-95509149	HRE	kidney:	n/a
47	chr1:95508854-95508904	NB4	blood:	n/a
48	chr1:95508854-95508904	PrEC	prostate:	n/a
49	chr1:95508854-95508904	HRCEpiC	kidney:	n/a
50	chr1:95509099-95509149	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:95519405..95521800-chr1:95524296..95526838,2	K562	blood:
2	chr1:95271098..95272014-chr1:95508742..95509603,4	MCF-7	breast:
3	chr1:95317605..95318348-chr1:95507244..95507950,2	MCF-7	breast:
4	chr1:95487503..95489480-chr1:95499680..95501424,2	MCF-7	breast:
5	chr1:95494947..95496682-chr1:95499857..95502061,2	K562	blood:
6	chr1:95318482..95319284-chr1:95507056..95507916,2	MCF-7	breast:
7	chr1:95319207..95320829-chr1:95507414..95509861,2	MCF-7	breast:
8	chr1:95507332..95508861-chr1:95511059..95512628,2	K562	blood:
9	chr1:95525449..95527054-chr1:95536002..95537685,2	MCF-7	breast:
10	chr1:95507332..95508861-chr1:95511059..95512628,2	K562	blood:
11	chr1:95517202..95518728-chr1:95521625..95524347,2	K562	blood:
12	chr1:95508625..95509695-chr1:95699228..95700102,5	K562	blood:
13	chr1:95517202..95518728-chr1:95521625..95524347,2	K562	blood:
14	chr1:95319740..95320605-chr1:95506874..95507813,4	MCF-7	breast:
15	chr1:95320267..95322937-chr1:95507219..95508813,2	K562	blood:
16	chr1:95319543..95320948-chr1:95506740..95507947,13	MCF-7	breast:
17	chr1:95319500..95321122-chr1:95506360..95508228,9	K562	blood:
18	chr1:95319373..95320645-chr1:95508673..95509610,12	MCF-7	breast:
19	chr1:95508689..95509241-chr9:134615140..134616062,2	MCF-7	breast:
20	chr1:95271063..95271580-chr1:95508693..95509648,2	K562	blood:
21	chr1:95285703..95286399-chr1:95508712..95509642,4	MCF-7	breast:
22	chr1:95285374..95286173-chr1:95508980..95509632,2	MCF-7	breast:
23	chr1:95318706..95321767-chr1:95507313..95510717,3	K562	blood:
24	chr1:95319681..95320573-chr1:95508384..95509568,5	MCF-7	breast:
25	chr1:95319172..95320847-chr1:95508664..95509618,15	K562	blood:
26	chr1:95519405..95521800-chr1:95524296..95526838,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM56-2	chr1:95527152-95527745	ENSG00000230427.1

Variant related genes	Relation type
ENSG00000230427	TF binding region
ENSG00000230427	CpG island
ENSG00000237416	chromatin interactions
ENSG00000122481	chromatin interactions
ENSG00000226026	chromatin interactions
ENSG00000107263	chromatin interactions
ENSG00000224081	chromatin interactions
ENSG00000143036	chromatin interactions

Extended variants
information (count: 994 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532138225	chr1:95501018-95501019	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs551973853	chr1:95501042-95501043	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565991450	chr1:95501055-95501056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs535127059	chr1:95501057-95501058	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs190167594	chr1:95501058-95501059	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs138778658	chr1:95501182-95501183	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs537470405	chr1:95501231-95501232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61772659	chr1:95501310-95501311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371694261	chr1:95501337-95501338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577629551	chr1:95501374-95501375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546392836	chr1:95501380-95501381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542597245	chr1:95501401-95501402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553610017	chr1:95501402-95501403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181681017	chr1:95501521-95501522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185683111	chr1:95501558-95501559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560870243	chr1:95501598-95501599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188830300	chr1:95501603-95501604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551513848	chr1:95501618-95501619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368664877	chr1:95501636-95501637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374782172	chr1:95501637-95501638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543027824	chr1:95501676-95501677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112790624	chr1:95501698-95501699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149381791	chr1:95501713-95501714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144657249	chr1:95501733-95501734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181293827	chr1:95501784-95501785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551910856	chr1:95501801-95501802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78289139	chr1:95501829-95501830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537065687	chr1:95501850-95501851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559489646	chr1:95501960-95501961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372877560	chr1:95501973-95501974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139765298	chr1:95501976-95501977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35068075	chr1:95502000-95502001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12121646	chr1:95502005-95502006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151255996	chr1:95502018-95502019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548659658	chr1:95502037-95502038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568501701	chr1:95502078-95502079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12749980	chr1:95502114-95502115	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs550996775	chr1:95502143-95502144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533545023	chr1:95502220-95502221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561794170	chr1:95502224-95502225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146165512	chr1:95502226-95502227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540150455	chr1:95502258-95502259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553422511	chr1:95502259-95502260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140121767	chr1:95502274-95502275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375035660	chr1:95502316-95502317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549656538	chr1:95502327-95502328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115016036	chr1:95502328-95502329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554611665	chr1:95502356-95502357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373226457	chr1:95502361-95502362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542988849	chr1:95502407-95502408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95480000-95508800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr1:95485200-95507000	Weak transcription	Fetal Heart	heart
3	chr1:95488000-95507000	Weak transcription	Ovary	ovary
4	chr1:95488200-95505400	Weak transcription	Pancreas	Pancrea
5	chr1:95488200-95507000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr1:95488200-95537600	Weak transcription	Right Ventricle	heart
7	chr1:95488400-95507000	Weak transcription	Brain Angular Gyrus	brain
8	chr1:95488400-95507800	Weak transcription	Brain Substantia Nigra	brain
9	chr1:95488600-95507800	Weak transcription	Colon Smooth Muscle	Colon
10	chr1:95488800-95505400	Weak transcription	Small Intestine	intestine
11	chr1:95489400-95517200	Weak transcription	Aorta	Aorta
12	chr1:95491400-95503600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr1:95491400-95507000	Weak transcription	Fetal Kidney	kidney
14	chr1:95491600-95529600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr1:95492600-95507800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:95492800-95504000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:95492800-95507000	Weak transcription	Fetal Stomach	stomach
18	chr1:95492800-95508800	Weak transcription	Primary T cells from cord blood	blood
19	chr1:95493400-95508800	Weak transcription	Liver	Liver
20	chr1:95495000-95504800	Weak transcription	Esophagus	oesophagus
21	chr1:95495200-95508000	Weak transcription	HepG2	liver
22	chr1:95495200-95508800	Weak transcription	Fetal Intestine Small	intestine
23	chr1:95495400-95503800	Weak transcription	Primary B cells from cord blood	blood
24	chr1:95495400-95505800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr1:95495400-95507000	Weak transcription	Fetal Muscle Leg	muscle
26	chr1:95497000-95508000	Weak transcription	Left Ventricle	heart
27	chr1:95497800-95501200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr1:95499000-95501800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:95499200-95501200	Enhancers	HSMMtube	muscle
30	chr1:95499200-95501200	Enhancers	NHDF-Ad	bronchial
31	chr1:95499200-95501800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:95499200-95501800	Enhancers	HSMM	muscle
33	chr1:95499200-95501800	Enhancers	NH-A	brain
34	chr1:95499200-95501800	Enhancers	Osteobl	bone
35	chr1:95499200-95502000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:95499400-95501400	Enhancers	NHLF	lung
37	chr1:95499400-95501800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:95499400-95501800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:95499400-95501800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:95499400-95501800	Enhancers	HMEC	breast
41	chr1:95499400-95501800	Enhancers	NHEK	skin
42	chr1:95499400-95502000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:95499400-95503200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:95499600-95502600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:95499800-95502600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr1:95500400-95501200	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:95500400-95501600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:95500400-95502600	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr1:95500600-95501000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:95500600-95507000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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