Variant report

Variant	esv2754686
Chromosome Location	chr1:114531958-114602958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:622)
CpG islands
(count:428)
Chromatin interactive
region (count:114)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:114564315-114564622	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:114576035-114576199	HepG2	liver:	n/a	n/a
3	ATF1	chr1:114552203-114552226	K562	blood:	n/a	n/a
4	ATF2	chr1:114575738-114576683	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:114574968-114575424	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:114575927-114576477	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:114584639-114584648	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr1:114575908-114575930	K562	blood:	n/a	n/a
9	BHLHE40	chr1:114552055-114552425	HepG2	liver:	n/a	n/a
10	BHLHE40	chr1:114590628-114590695	K562	blood:	n/a	n/a
11	CEBPB	chr1:114583000-114583220	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:114552076-114552394	IMR90	lung:	n/a	chr1:114552220-114552231
13	CEBPB	chr1:114562388-114562667	K562	blood:	n/a	chr1:114562534-114562545
14	CEBPB	chr1:114562440-114562643	HepG2	liver:	n/a	chr1:114562534-114562545
15	CEBPB	chr1:114564277-114564542	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:114583028-114583252	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:114545512-114545840	IMR90	lung:	n/a	chr1:114545666-114545677
18	CEBPB	chr1:114557482-114558308	HCT-116	colon:	n/a	n/a
19	CEBPB	chr1:114566718-114567014	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:114576901-114577091	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:114540465-114540585	HepG2	liver:	n/a	chr1:114540504-114540515
22	CEBPB	chr1:114552086-114552364	HepG2	liver:	n/a	chr1:114552220-114552231
23	CEBPB	chr1:114577025-114577200	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:114557824-114558018	A549	lung:	n/a	n/a
25	CEBPB	chr1:114557604-114558136	A549	lung:	n/a	n/a
26	CEBPB	chr1:114562456-114562617	Hela-S3	cervix:	n/a	chr1:114562534-114562545
27	CEBPB	chr1:114545594-114545838	HepG2	liver:	n/a	chr1:114545666-114545677
28	CEBPB	chr1:114562390-114562651	IMR90	lung:	n/a	chr1:114562534-114562545
29	CHD1	chr1:114580353-114581122	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr1:114574382-114574437	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr1:114575803-114577310	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr1:114534404-114534455	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr1:114577475-114577934	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr1:114575922-114576210	A549	lung:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
35	CTCF	chr1:114576000-114576150	AG04450	lung:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
36	CTCF	chr1:114576000-114576150	HRPEpiC	eye:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
37	CTCF	chr1:114575995-114576160	GM10266	blood:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
38	CTCF	chr1:114576000-114576150	NHLF	lung:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
39	CTCF	chr1:114544120-114544270	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr1:114576000-114576150	HepG2	liver:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
41	CTCF	chr1:114575994-114576217	LNCaP	prostate:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
42	CTCF	chr1:114575943-114576212	GM12878	blood:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
43	CTCF	chr1:114576000-114576150	HPAF	blood vessel:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
44	CTCF	chr1:114544080-114544230	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr1:114575982-114576160	GM13977	blood:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
46	CTCF	chr1:114575933-114576215	MCF-7	breast:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
47	CTCF	chr1:114592380-114592530	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:114576000-114576150	GM12871	blood:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
49	CTCF	chr1:114576080-114576230	HUVEC	blood vessel:	n/a	chr1:114576083-114576099 chr1:114576085-114576094 chr1:114576084-114576105
50	CTCF	chr1:114563060-114563210	WERI-Rb-1	eye:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:114544915-114544965	AG09319	gingival:	n/a
2	chr1:114544915-114544965	AG09319	gingival:	n/a
3	chr1:114566249-114566299	SKMC	muscle:	n/a
4	chr1:114576186-114576236	HUVEC	blood vessel:	n/a
5	chr1:114544815-114544865	HNPCEpiC	eye:	n/a
6	chr1:114566249-114566299	AG10803	skin:	n/a
7	chr1:114566249-114566299	NHBE	bronchial:	n/a
8	chr1:114566249-114566299	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:114566249-114566299	HRE	kidney:	n/a
10	chr1:114580856-114580906	T-47D	breast:	n/a
11	chr1:114576186-114576236	K562	blood:	n/a
12	chr1:114545478-114545528	SKMC	muscle:	n/a
13	chr1:114545478-114545528	SAEC	small airway:	n/a
14	chr1:114576186-114576236	PFSK-1	brain:	n/a
15	chr1:114576186-114576236	HepG2	liver:	n/a
16	chr1:114544815-114544865	SK-N-SH	brain:	n/a
17	chr1:114544915-114544965	HEEpiC	esophagus:	n/a
18	chr1:114544815-114544865	HCPEpiC	choroid plexus:	n/a
19	chr1:114580856-114580906	NB4	blood:	n/a
20	chr1:114544815-114544865	AG04449	skin:	fetal
21	chr1:114592384-114592434	SK-N-SH	brain:	n/a
22	chr1:114580856-114580906	GM12892	blood:	n/a
23	chr1:114592384-114592434	T-47D	breast:	n/a
24	chr1:114576186-114576236	AG10803	skin:	n/a
25	chr1:114544915-114544965	HCF	heart:	n/a
26	chr1:114576186-114576236	A549	lung:	n/a
27	chr1:114544915-114544965	H1-hESC	embryonic stem cell:	embryo
28	chr1:114580856-114580906	NH-A	brain:	n/a
29	chr1:114592384-114592434	PANC-1	pancreas:	n/a
30	chr1:114545478-114545528	SK-N-SH_RA	brain:	n/a
31	chr1:114544915-114544965	NH-A	brain:	n/a
32	chr1:114545478-114545528	GM12878	blood:	n/a
33	chr1:114544915-114544965	NHDF-neo	bronchial:	n/a
34	chr1:114545478-114545528	RPTEC	kidney:	n/a
35	chr1:114576186-114576236	MCF10A-Er-Src	breast:	n/a
36	chr1:114576186-114576236	Hela-S3	cervix:	n/a
37	chr1:114566249-114566299	PFSK-1	brain:	n/a
38	chr1:114576186-114576236	BJ	skin:	n/a
39	chr1:114545478-114545528	HCM	heart:	n/a
40	chr1:114592384-114592434	HEK293	kidney:	embryo
41	chr1:114544915-114544965	HMEC	breast:	n/a
42	chr1:114580856-114580906	HCT-116	colon:	n/a
43	chr1:114544815-114544865	HEK293	kidney:	embryo
44	chr1:114580856-114580906	NHDF-neo	bronchial:	n/a
45	chr1:114592384-114592434	GM12878	blood:	n/a
46	chr1:114544915-114544965	BJ	skin:	n/a
47	chr1:114545478-114545528	T-47D	breast:	n/a
48	chr1:114592384-114592434	K562	blood:	n/a
49	chr1:114566249-114566299	HAEpiC	amniotic membrane:	n/a
50	chr1:114576186-114576236	IMR90	lung:	fetal

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:114575984..114576551-chr16:67189207..67189812,2	MCF-7	breast:
2	chr1:114524848..114527263-chr1:114536709..114538580,2	MCF-7	breast:
3	chr1:114565136..114566738-chr1:114579035..114581815,2	MCF-7	breast:
4	chr1:114575470..114578189-chr1:114589215..114591996,2	MCF-7	breast:
5	chr1:114574403..114579108-chr1:114596233..114599527,4	MCF-7	breast:
6	chr1:114542743..114543294-chr1:114576534..114577039,2	MCF-7	breast:
7	chr1:114525379..114527622-chr1:114550008..114552290,2	MCF-7	breast:
8	chr1:114542012..114545374-chr1:114546665..114550034,4	K562	blood:
9	chr1:114519300..114519841-chr1:114585412..114586240,2	MCF-7	breast:
10	chr1:114544161..114545963-chr1:114548687..114551094,2	MCF-7	breast:
11	chr1:114543887..114546791-chr1:114577396..114579805,2	MCF-7	breast:
12	chr1:114534999..114536807-chr1:114545965..114547764,2	K562	blood:
13	chr1:114575647..114576555-chr1:114825189..114826082,7	MCF-7	breast:
14	chr1:114518951..114519800-chr1:114576379..114577180,4	MCF-7	breast:
15	chr1:114563454..114565065-chr1:114613996..114616679,2	MCF-7	breast:
16	chr1:114534979..114536505-chr1:114575410..114577560,2	MCF-7	breast:
17	chr1:114577897..114580371-chr1:114581560..114584344,2	MCF-7	breast:
18	chr1:114472223..114474448-chr1:114554787..114556882,2	K562	blood:
19	chr1:114590926..114593498-chr1:114625359..114627730,2	MCF-7	breast:
20	chr1:114594128..114597061-chr1:114598670..114602014,3	K562	blood:
21	chr1:114534999..114536807-chr1:114545965..114547764,2	K562	blood:
22	chr1:114589518..114591108-chr3:138330030..138332781,2	MCF-7	breast:
23	chr1:114519045..114519788-chr1:114576300..114577157,2	MCF-7	breast:
24	chr1:114576305..114576992-chr1:114632415..114633398,6	MCF-7	breast:
25	chr1:114557212..114558727-chr1:114559009..114561477,2	MCF-7	breast:
26	chr1:114596275..114599885-chr1:114602118..114604793,4	MCF-7	breast:
27	chr1:114534979..114536505-chr1:114575410..114577560,2	MCF-7	breast:
28	chr1:114565150..114566760-chr1:114567203..114568734,2	MCF-7	breast:
29	chr1:114553668..114556667-chr1:114558586..114560264,2	MCF-7	breast:
30	chr1:114530146..114532962-chr1:114538190..114540819,2	MCF-7	breast:
31	chr1:114557212..114558727-chr1:114559009..114561477,2	MCF-7	breast:
32	chr1:114576357..114577173-chr1:114585486..114586359,3	MCF-7	breast:
33	chr1:114585196..114589086-chr1:114619214..114622779,3	MCF-7	breast:
34	chr1:114546630..114549912-chr1:114550088..114553437,4	MCF-7	breast:
35	chr1:114563136..114568125-chr1:114568802..114572804,6	MCF-7	breast:
36	chr1:114546364..114550367-chr1:114550390..114555029,5	MCF-7	breast:
37	chr1:114542743..114543294-chr1:114576534..114577039,2	MCF-7	breast:
38	chr1:114577056..114579380-chr1:114582977..114584723,3	MCF-7	breast:
39	chr1:114532816..114535343-chr1:114801379..114803546,2	MCF-7	breast:
40	chr1:114576357..114577173-chr1:114585486..114586359,3	MCF-7	breast:
41	chr1:114519027..114521459-chr1:114540570..114543395,2	MCF-7	breast:
42	chr1:114577897..114580371-chr1:114581560..114584344,2	MCF-7	breast:
43	chr1:114555472..114558426-chr1:114586301..114588819,2	MCF-7	breast:
44	chr1:114519655..114520167-chr1:114575158..114576111,2	MCF-7	breast:
45	chr1:114575592..114576473-chr1:114761828..114762361,2	MCF-7	breast:
46	chr1:114542012..114544425-chr1:114548121..114550034,2	K562	blood:
47	chr1:114591094..114593001-chr1:114597614..114600452,2	K562	blood:
48	chr1:114551859..114553790-chr1:114563560..114565413,2	MCF-7	breast:
49	chr1:114576041..114576656-chr1:114804475..114805150,2	MCF-7	breast:
50	chr1:114523401..114526223-chr1:114556190..114558490,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFML3-2	chr1:114577818-114578381	NONHSAT005352
2	lnc-SYT6-2	chr1:114564551-114564752	NONHSAT005350
3	lnc-SYT6-2	chr1:114569348-114569456	NONHSAT005351
4	lnc-SYT6-2	chr1:114564551-114564666	NONHSAT005351
5	lnc-SYT6-2	chr1:114565302-114565402	NONHSAT005351
6	lnc-OLFML3-3	chr1:114550572-114550830	NONHSAT005349
7	lnc-SYT6-2	chr1:114574656-114574814	NONHSAT005351
8	lnc-SYT6-2	chr1:114557425-114557791	NONHSAT005350
9	lnc-OLFML3-2	chr1:114574961-114577268	NONHSAT005352
10	lnc-SYT6-2	chr1:114557545-114557791	NONHSAT005351

No data

Variant related genes	Relation type
ENSG00000270780	TF binding region
ENSG00000270780	CpG island
ENSG00000135722	chromatin interactions
ENSG00000270780	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000102871	chromatin interactions
ENSG00000232895	chromatin interactions
ENSG00000116774	chromatin interactions
ENSG00000214336	chromatin interactions
ENSG00000083223	chromatin interactions

Extended variants
information (count: 2665 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2665 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76581814	chr1:114531963-114531964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184874717	chr1:114531966-114531967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550869213	chr1:114531982-114531983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531420002	chr1:114532028-114532029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3007014	chr1:114532097-114532098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs530123530	chr1:114532101-114532102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547101196	chr1:114532102-114532103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566869269	chr1:114532128-114532129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539077047	chr1:114532131-114532132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559000983	chr1:114532145-114532146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116000340	chr1:114532158-114532159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538162927	chr1:114532178-114532179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140720328	chr1:114532216-114532217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574608329	chr1:114532250-114532251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530060640	chr1:114532282-114532283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs905598	chr1:114532307-114532308	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs374184827	chr1:114532345-114532346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373493558	chr1:114532351-114532352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144465206	chr1:114532367-114532368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376898209	chr1:114532396-114532397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545351201	chr1:114532405-114532406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35730746	chr1:114532423-114532424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189632383	chr1:114532428-114532429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17032085	chr1:114532457-114532458	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs544926157	chr1:114532477-114532478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374551970	chr1:114532496-114532497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530367633	chr1:114532507-114532508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149674754	chr1:114532518-114532519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201510251	chr1:114532521-114532522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs58043788	chr1:114532522-114532523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7549714	chr1:114532523-114532524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs72102458	chr1:114532531-114532532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560530739	chr1:114532537-114532538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532655869	chr1:114532538-114532539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397957192	chr1:114532542-114532543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2359003	chr1:114532543-114532544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs905597	chr1:114532544-114532545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs67251529	chr1:114532547-114532548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs3007015	chr1:114532548-114532549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140062653	chr1:114532564-114532565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569288882	chr1:114532656-114532657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115661874	chr1:114532659-114532660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75868822	chr1:114532670-114532671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568156452	chr1:114532716-114532717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186218991	chr1:114532755-114532756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76679620	chr1:114532804-114532805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150290708	chr1:114532829-114532830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191034267	chr1:114532833-114532834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116168799	chr1:114532850-114532851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373235436	chr1:114532883-114532884	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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114523800-114534600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:114527800-114533000	Weak transcription	HSMMtube	muscle
3	chr1:114528000-114533400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr1:114528000-114536600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:114528200-114535800	Weak transcription	Fetal Muscle Trunk	muscle
6	chr1:114528200-114540800	Weak transcription	Fetal Lung	lung
7	chr1:114530000-114536200	Weak transcription	Fetal Stomach	stomach
8	chr1:114530200-114533000	Weak transcription	Fetal Muscle Leg	muscle
9	chr1:114531600-114532200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:114532200-114535800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr1:114533000-114533600	Enhancers	Fetal Muscle Leg	muscle
12	chr1:114533000-114533800	Enhancers	HSMMtube	muscle
13	chr1:114533400-114534600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr1:114533600-114534600	Weak transcription	Fetal Muscle Leg	muscle
15	chr1:114534600-114535200	Enhancers	Fetal Muscle Leg	muscle
16	chr1:114535200-114536200	Weak transcription	Fetal Muscle Leg	muscle
17	chr1:114535400-114536000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:114535600-114536000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:114535600-114536600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:114535800-114536400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:114535800-114536600	Enhancers	Fetal Muscle Trunk	muscle
22	chr1:114536200-114536400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:114536600-114536800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:114536600-114537000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:114536800-114537000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:114537400-114542200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:114537600-114537800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:114538600-114538800	ZNF genes & repeats	Right Atrium	heart
29	chr1:114538800-114545800	Weak transcription	Right Atrium	heart
30	chr1:114540200-114540400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr1:114540400-114543000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:114540800-114541200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:114540800-114541400	Enhancers	Fetal Stomach	stomach
34	chr1:114540800-114542000	Enhancers	Fetal Lung	lung
35	chr1:114541000-114541200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:114541000-114541200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:114541000-114541200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:114541000-114541200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:114541000-114541200	Bivalent Enhancer	HUVEC	blood vessel
40	chr1:114541000-114541400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:114541000-114541400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:114541000-114541600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:114541000-114542400	Enhancers	Fetal Muscle Leg	muscle
44	chr1:114541200-114541800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr1:114541200-114542200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:114541200-114544200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:114541200-114544800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:114541200-114545200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:114541400-114542800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr1:114541400-114545000	Weak transcription	Fetal Stomach	stomach

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