Variant report

Variant	esv3395760
Chromosome Location	chr9:140444631-140447079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:870)
CpG islands
(count:427)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:870 , 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	ATF3	chr9:140444794-140445032	K562	blood:	n/a	n/a
2	BACH1	chr9:140445891-140445908	K562	blood:	n/a	n/a
3	BACH1	chr9:140445812-140446093	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:140444871-140445043	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr9:140446470-140447336	A549	lung:	n/a	chr9:140446514-140446527
6	BCL3	chr9:140446495-140447277	A549	lung:	n/a	chr9:140446514-140446527
7	BCLAF1	chr9:140446664-140447061	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:140445821-140446098	K562	blood:	n/a	chr9:140445881-140445897
9	BHLHE40	chr9:140444689-140445061	HepG2	liver:	n/a	n/a
10	BHLHE40	chr9:140446341-140446464	K562	blood:	n/a	n/a
11	BHLHE40	chr9:140444731-140445029	A549	lung:	n/a	n/a
12	BHLHE40	chr9:140444679-140445082	K562	blood:	n/a	n/a
13	BHLHE40	chr9:140445842-140446042	GM12878	blood:	n/a	chr9:140445881-140445897
14	BHLHE40	chr9:140444730-140445039	GM12878	blood:	n/a	n/a
15	BRCA1	chr9:140445938-140446071	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:140444741-140444956	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr9:140444784-140445046	K562	blood:	n/a	n/a
18	CBX3	chr9:140446570-140447020	K562	blood:	n/a	n/a
19	CBX3	chr9:140445754-140446101	K562	blood:	n/a	n/a
20	CCNT2	chr9:140445684-140446909	K562	blood:	n/a	n/a
21	CCNT2	chr9:140444833-140444990	K562	blood:	n/a	n/a
22	CEBPB	chr9:140445888-140445963	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:140446756-140446772	K562	blood:	n/a	n/a
24	CEBPD	chr9:140446183-140446577	HepG2	liver:	n/a	n/a
25	CHD1	chr9:140446424-140446648	GM12878	blood:	n/a	n/a
26	CHD1	chr9:140446613-140446783	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr9:140444778-140445068	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr9:140445738-140446999	GM12878	blood:	n/a	n/a
29	CHD2	chr9:140445897-140446058	HepG2	liver:	n/a	n/a
30	CHD2	chr9:140445726-140446611	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr9:140446911-140446947	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr9:140445921-140447101	K562	blood:	n/a	n/a
33	CHD2	chr9:140446217-140446497	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr9:140446311-140446853	HepG2	liver:	n/a	n/a
35	CREB1	chr9:140446182-140447240	HepG2	liver:	n/a	n/a
36	CREB1	chr9:140445710-140446093	A549	lung:	n/a	n/a
37	CREB1	chr9:140446187-140446937	A549	lung:	n/a	n/a
38	CREB1	chr9:140446174-140446540	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr9:140445960-140446110	GM12801	blood:	n/a	chr9:140446018-140446031
40	CTCF	chr9:140445972-140446079	HUVEC	blood vessel:	n/a	chr9:140446018-140446031
41	CTCF	chr9:140445884-140446087	SK-N-SH_RA	brain:	n/a	chr9:140446018-140446031
42	CTCF	chr9:140445539-140446291	MCF-7	breast:	n/a	chr9:140446018-140446031
43	CTCF	chr9:140445960-140446110	Hela-S3	cervix:	n/a	chr9:140446018-140446031
44	CTCF	chr9:140445920-140446070	HFF-Myc	foreskin:	n/a	chr9:140446018-140446031
45	CTCF	chr9:140445920-140446070	HPF	lung:	n/a	chr9:140446018-140446031
46	CTCF	chr9:140444880-140445030	AG04449	skin:	n/a	n/a
47	CTCF	chr9:140445889-140446138	MCF-7	breast:	n/a	chr9:140446018-140446031
48	CTCF	chr9:140446760-140446910	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr9:140445980-140446130	HVMF	connective:	n/a	chr9:140446018-140446031
50	CTCF	chr9:140445940-140446090	Caco-2	colon:	n/a	chr9:140446018-140446031

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140446656-140446706	H1-hESC	embryonic stem cell:	embryo
2	chr9:140446656-140446706	ProgFib	skin:	n/a
3	chr9:140444966-140445016	HIPEpiC	eye:	n/a
4	chr9:140446240-140446290	SK-N-SH	brain:	n/a
5	chr9:140446656-140446706	HepG2	liver:	n/a
6	chr9:140446656-140446706	HUVEC	blood vessel:	n/a
7	chr9:140445760-140445810	IMR90	lung:	fetal
8	chr9:140446823-140446873	PANC-1	pancreas:	n/a
9	chr9:140446240-140446290	U87	brain:	n/a
10	chr9:140446240-140446290	NHDF-neo	bronchial:	n/a
11	chr9:140446993-140447043	HEEpiC	esophagus:	n/a
12	chr9:140445760-140445810	NH-A	brain:	n/a
13	chr9:140445760-140445810	NHDF-neo	bronchial:	n/a
14	chr9:140446458-140446508	HEEpiC	esophagus:	n/a
15	chr9:140446240-140446290	T-47D	breast:	n/a
16	chr9:140445760-140445810	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:140446656-140446706	NT2-D1	testis:	n/a
18	chr9:140446993-140447043	SK-N-MC	brain:	n/a
19	chr9:140445760-140445810	HL-60	blood:	n/a
20	chr9:140446240-140446290	LNCaP	prostate:	n/a
21	chr9:140446240-140446290	AG10803	skin:	n/a
22	chr9:140446458-140446508	AG10803	skin:	n/a
23	chr9:140446458-140446508	CMK	blood:	n/a
24	chr9:140445760-140445810	HNPCEpiC	eye:	n/a
25	chr9:140444966-140445016	GM12878	blood:	n/a
26	chr9:140446823-140446873	MCF-7	breast:	n/a
27	chr9:140446240-140446290	PANC-1	pancreas:	n/a
28	chr9:140446240-140446290	ProgFib	skin:	n/a
29	chr9:140446993-140447043	U87	brain:	n/a
30	chr9:140445760-140445810	BE2_C	brain:	n/a
31	chr9:140444966-140445016	GM06990	blood:	n/a
32	chr9:140445760-140445810	HAEpiC	amniotic membrane:	n/a
33	chr9:140446823-140446873	CMK	blood:	n/a
34	chr9:140446823-140446873	GM12891	blood:	n/a
35	chr9:140446993-140447043	SK-N-SH	brain:	n/a
36	chr9:140444966-140445016	CMK	blood:	n/a
37	chr9:140445760-140445810	Caco-2	colon:	n/a
38	chr9:140446458-140446508	HMEC	breast:	n/a
39	chr9:140446823-140446873	HRCEpiC	kidney:	n/a
40	chr9:140446823-140446873	PrEC	prostate:	n/a
41	chr9:140444966-140445016	U87	brain:	n/a
42	chr9:140446823-140446873	HUVEC	blood vessel:	n/a
43	chr9:140444966-140445016	SK-N-SH_RA	brain:	n/a
44	chr9:140444966-140445016	A549	lung:	n/a
45	chr9:140446823-140446873	HMEC	breast:	n/a
46	chr9:140446458-140446508	HepG2	liver:	n/a
47	chr9:140446458-140446508	HL-60	blood:	n/a
48	chr9:140446240-140446290	HRCEpiC	kidney:	n/a
49	chr9:140446240-140446290	SK-N-MC	brain:	n/a
50	chr9:140446823-140446873	HL-60	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140444986..140448753-chr9:140497892..140501428,4	K562	blood:
2	chr9:140443433..140448155-chr9:140497818..140502870,8	MCF-7	breast:
3	chr19:48281795..48283367-chr9:140445657..140447919,2	MCF-7	breast:
4	chr9:140445810..140448101-chr9:140449501..140452314,4	K562	blood:
5	chr9:140445818..140448729-chr9:140451345..140453162,4	MCF-7	breast:
6	chr9:140188507..140191128-chr9:140444764..140447765,3	MCF-7	breast:
7	chr9:140444476..140446866-chr9:140469262..140473127,6	MCF-7	breast:
8	chr9:140130666..140131228-chr9:140445991..140446498,2	K562	blood:
9	chr9:140444528..140447263-chr9:140504669..140508200,5	MCF-7	breast:
10	chr9:140081713..140085345-chr9:140445556..140447863,3	MCF-7	breast:
11	chr9:140189775..140190406-chr9:140445582..140446845,3	K562	blood:
12	chr9:140444557..140448587-chr9:140470804..140473699,6	MCF-7	breast:
13	chr9:140317304..140318861-chr9:140444413..140447408,2	K562	blood:
14	chr9:140118466..140120300-chr9:140443395..140446342,2	MCF-7	breast:
15	chr9:140352080..140354787-chr9:140444624..140448715,3	MCF-7	breast:
16	chr9:140446189..140447738-chr9:140484697..140486582,2	K562	blood:
17	chr9:140171323..140173620-chr9:140444809..140447880,3	K562	blood:
18	chr9:140444420..140448721-chr9:140471876..140474832,3	K562	blood:
19	chr9:140395969..140398056-chr9:140445670..140447895,2	K562	blood:
20	chr8:135112230..135113008-chr9:140445827..140446528,2	MCF-7	breast:
21	chr14:81687170..81687965-chr9:140446133..140446842,2	Hela-S3	cervix:
22	chr9:140189588..140190355-chr9:140445590..140446295,2	MCF-7	breast:
23	chr9:140446439..140449718-chr9:140469897..140473461,3	K562	blood:
24	chr9:140441799..140446269-chr9:140505086..140508400,5	MCF-7	breast:
25	chr9:140447049..140448753-chr9:140497892..140500070,2	K562	blood:
26	chr9:140443479..140444983-chr9:140499290..140501657,2	K562	blood:
27	chr9:140443274..140446260-chr9:140471876..140474598,3	K562	blood:
28	chr9:140439935..140442817-chr9:140445009..140447280,2	MCF-7	breast:
29	chr9:140193137..140197903-chr9:140443164..140449787,14	MCF-7	breast:
30	chr9:140355494..140357648-chr9:140446528..140449268,2	K562	blood:
31	chr9:140188389..140190191-chr9:140444959..140446807,2	MCF-7	breast:
32	chr9:140170828..140173620-chr9:140446274..140448338,3	K562	blood:
33	chr9:140444243..140447461-chr9:140473220..140477204,4	MCF-7	breast:
34	chr9:140445002..140446703-chr9:140512317..140515053,2	MCF-7	breast:
35	chr9:140443475..140446294-chr9:140484220..140486836,3	MCF-7	breast:
36	chr9:140444995..140447677-chr9:140508337..140511208,2	MCF-7	breast:
37	chr9:140205840..140207870-chr9:140446473..140449405,2	MCF-7	breast:
38	chr9:140444055..140447780-chr9:140498087..140502451,7	MCF-7	breast:

No data

Variant related genes	Relation type
PNPLA7	TF binding region
MRPL41	TF binding region
PNPLA7	CpG island
MRPL41	CpG island
ENSG00000130653	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000263933	chromatin interactions
ENSG00000176248	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000188747	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000176101	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000178980	chromatin interactions
ENSG00000197191	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000198113	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374861102	chr9:140444635-140444636	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs78784297	chr9:140444651-140444652	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs377724383	chr9:140444659-140444660	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs116310481	chr9:140444678-140444679	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs140509962	chr9:140444711-140444712	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs575671549	chr9:140444754-140444755	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs544927252	chr9:140444768-140444769	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs553265661	chr9:140444779-140444780	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs555349138	chr9:140444817-140444818	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs368320212	chr9:140444851-140444852	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs540857590	chr9:140444893-140444894	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs560500405	chr9:140444966-140444967	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs142791311	chr9:140444988-140444989	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs544663451	chr9:140445024-140445025	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
15	rs202128325	chr9:140445070-140445071	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
16	rs13299241	chr9:140445079-140445080	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs113188013	chr9:140445167-140445168	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs113659841	chr9:140445183-140445184	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs371394917	chr9:140445584-140445585	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
20	rs111730524	chr9:140445648-140445649	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
21	rs540617905	chr9:140445654-140445655	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
22	rs550149458	chr9:140445669-140445670	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
23	rs567582963	chr9:140445697-140445698	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
24	rs374785555	chr9:140445737-140445738	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
25	rs546793434	chr9:140445765-140445766	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
26	rs566516408	chr9:140445823-140445824	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
27	rs4308848	chr9:140445849-140445850	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
28	rs115681155	chr9:140445871-140445872	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
29	rs569373144	chr9:140445881-140445882	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
30	rs538283299	chr9:140445894-140445895	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
31	rs554987472	chr9:140445895-140445896	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
32	rs575105947	chr9:140446043-140446044	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
33	rs367780333	chr9:140446050-140446051	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
34	rs371179222	chr9:140446090-140446091	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs371615488	chr9:140446101-140446102	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
36	rs540543550	chr9:140446124-140446125	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
37	rs528392577	chr9:140446141-140446142	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs554352249	chr9:140446157-140446158	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
39	rs577319040	chr9:140446171-140446172	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
40	rs545983963	chr9:140446172-140446173	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
41	rs564678638	chr9:140446347-140446348	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
42	rs147383075	chr9:140446357-140446358	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
43	rs543830323	chr9:140446399-140446400	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
44	rs560691288	chr9:140446407-140446408	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs530015471	chr9:140446411-140446412	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs13289623	chr9:140446456-140446457	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
47	rs13289628	chr9:140446463-140446464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
48	rs369439866	chr9:140446558-140446559	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
49	rs373518805	chr9:140446627-140446628	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
50	rs13783	chr9:140446633-140446634	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140431800-140444800	Weak transcription	Dnd41	blood
2	chr9:140442000-140445000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr9:140443200-140444800	Enhancers	Spleen	Spleen
4	chr9:140443400-140445000	Enhancers	Fetal Heart	heart
5	chr9:140444000-140444800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:140444000-140444800	Flanking Active TSS	Brain Cingulate Gyrus	brain
7	chr9:140444000-140444800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr9:140444000-140445000	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr9:140444000-140445000	Flanking Active TSS	Primary B cells from peripheral blood	blood
10	chr9:140444000-140445000	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr9:140444000-140445000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr9:140444000-140447200	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr9:140444200-140444800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:140444200-140444800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:140444200-140444800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:140444200-140444800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr9:140444200-140444800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr9:140444200-140444800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:140444200-140444800	Flanking Active TSS	Brain Angular Gyrus	brain
20	chr9:140444200-140444800	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr9:140444200-140444800	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr9:140444200-140444800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr9:140444200-140444800	Flanking Active TSS	Colonic Mucosa	Colon
24	chr9:140444200-140444800	Flanking Active TSS	Duodenum Mucosa	Duodenum
25	chr9:140444200-140444800	Flanking Active TSS	Fetal Intestine Small	intestine
26	chr9:140444200-140444800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr9:140444200-140444800	Flanking Active TSS	Rectal Smooth Muscle	rectum
28	chr9:140444200-140445000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:140444200-140445000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr9:140444200-140445000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:140444200-140445000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:140444200-140445000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:140444200-140445000	Flanking Active TSS	Liver	Liver
34	chr9:140444200-140445000	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr9:140444200-140445000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr9:140444200-140445000	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr9:140444200-140445000	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr9:140444200-140445000	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr9:140444200-140445000	Flanking Active TSS	GM12878-XiMat	blood
40	chr9:140444200-140445000	Flanking Active TSS	Hela-S3	cervix
41	chr9:140444200-140445000	Flanking Active TSS	HepG2	liver
42	chr9:140444200-140445000	Enhancers	HMEC	breast
43	chr9:140444200-140445200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:140444200-140445600	Enhancers	Placenta	Placenta
45	chr9:140444400-140444800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr9:140444400-140444800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr9:140444400-140444800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:140444400-140444800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:140444400-140444800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:140444400-140444800	Flanking Active TSS	Primary T cells from cord blood	blood

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