Variant report

Variant	esv3370668
Chromosome Location	chr9:140444156-140447004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:876)
CpG islands
(count:489)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:876 , 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	chr9:140444871-140445043	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:140445812-140446093	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:140445891-140445908	K562	blood:	n/a	n/a
5	BCL3	chr9:140446495-140447277	A549	lung:	n/a	chr9:140446514-140446527
6	BCL3	chr9:140446470-140447336	A549	lung:	n/a	chr9:140446514-140446527
7	BCLAF1	chr9:140446664-140447061	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:140445842-140446042	GM12878	blood:	n/a	chr9:140445881-140445897
9	BHLHE40	chr9:140444679-140445082	K562	blood:	n/a	n/a
10	BHLHE40	chr9:140445821-140446098	K562	blood:	n/a	chr9:140445881-140445897
11	BHLHE40	chr9:140444730-140445039	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:140444689-140445061	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:140446341-140446464	K562	blood:	n/a	n/a
14	BHLHE40	chr9:140444731-140445029	A549	lung:	n/a	n/a
15	BRCA1	chr9:140444741-140444956	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:140445938-140446071	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr9:140445754-140446101	K562	blood:	n/a	n/a
18	CBX3	chr9:140444784-140445046	K562	blood:	n/a	n/a
19	CBX3	chr9:140446570-140447020	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	chr9:140446756-140446772	K562	blood:	n/a	n/a
23	CEBPB	chr9:140445888-140445963	Hela-S3	cervix:	n/a	n/a
24	CEBPD	chr9:140446183-140446577	HepG2	liver:	n/a	n/a
25	CHD1	chr9:140446613-140446783	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr9:140446424-140446648	GM12878	blood:	n/a	n/a
27	CHD2	chr9:140446911-140446947	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr9:140445921-140447101	K562	blood:	n/a	n/a
29	CHD2	chr9:140446217-140446497	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr9:140444778-140445068	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr9:140445726-140446611	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr9:140446311-140446853	HepG2	liver:	n/a	n/a
33	CHD2	chr9:140445897-140446058	HepG2	liver:	n/a	n/a
34	CHD2	chr9:140445738-140446999	GM12878	blood:	n/a	n/a
35	CREB1	chr9:140446174-140446540	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr9:140446182-140447240	HepG2	liver:	n/a	n/a
37	CREB1	chr9:140445710-140446093	A549	lung:	n/a	n/a
38	CREB1	chr9:140446187-140446937	A549	lung:	n/a	n/a
39	CTCF	chr9:140444742-140444967	K562	blood:	n/a	n/a
40	CTCF	chr9:140445920-140446070	AG09319	gingival:	n/a	chr9:140446018-140446031
41	CTCF	chr9:140445745-140446070	A549	lung:	n/a	chr9:140446018-140446031
42	CTCF	chr9:140445980-140446130	AG04450	lung:	n/a	chr9:140446018-140446031
43	CTCF	chr9:140444880-140445030	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr9:140445797-140446208	K562	blood:	n/a	chr9:140446018-140446031
45	CTCF	chr9:140445902-140446111	GM12878	blood:	n/a	chr9:140446018-140446031
46	CTCF	chr9:140445913-140446094	LNCaP	prostate:	n/a	chr9:140446018-140446031
47	CTCF	chr9:140445716-140446125	HCT-116	colon:	n/a	chr9:140446018-140446031
48	CTCF	chr9:140445620-140445770	HEK293	kidney:	n/a	n/a
49	CTCF	chr9:140445940-140446090	HFF-Myc	foreskin:	n/a	chr9:140446018-140446031
50	CTCF	chr9:140445940-140446090	AoAF	blood vessel:	n/a	chr9:140446018-140446031

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140445760-140445810	GM12892	blood:	n/a
2	chr9:140445760-140445810	GM12892	blood:	n/a
3	chr9:140444378-140444428	AG09319	gingival:	n/a
4	chr9:140446240-140446290	HIPEpiC	eye:	n/a
5	chr9:140446458-140446508	HAEpiC	amniotic membrane:	n/a
6	chr9:140446993-140447043	Caco-2	colon:	n/a
7	chr9:140446993-140447043	GM12891	blood:	n/a
8	chr9:140446993-140447043	NHBE	bronchial:	n/a
9	chr9:140444378-140444428	GM06990	blood:	n/a
10	chr9:140446993-140447043	HMEC	breast:	n/a
11	chr9:140446823-140446873	RPTEC	kidney:	n/a
12	chr9:140444966-140445016	HepG2	liver:	n/a
13	chr9:140444378-140444428	AG04449	skin:	fetal
14	chr9:140444966-140445016	HAEpiC	amniotic membrane:	n/a
15	chr9:140445760-140445810	HCPEpiC	choroid plexus:	n/a
16	chr9:140446656-140446706	HCPEpiC	choroid plexus:	n/a
17	chr9:140446656-140446706	AG10803	skin:	n/a
18	chr9:140445760-140445810	SKMC	muscle:	n/a
19	chr9:140444378-140444428	HUVEC	blood vessel:	n/a
20	chr9:140444966-140445016	BE2_C	brain:	n/a
21	chr9:140446240-140446290	GM06990	blood:	n/a
22	chr9:140446656-140446706	GM06990	blood:	n/a
23	chr9:140445760-140445810	HRE	kidney:	n/a
24	chr9:140446656-140446706	CMK	blood:	n/a
25	chr9:140446458-140446508	SAEC	small airway:	n/a
26	chr9:140444378-140444428	HNPCEpiC	eye:	n/a
27	chr9:140446993-140447043	MCF10A-Er-Src	breast:	n/a
28	chr9:140444966-140445016	A549	lung:	n/a
29	chr9:140446240-140446290	SK-N-SH_RA	brain:	n/a
30	chr9:140444378-140444428	RPTEC	kidney:	n/a
31	chr9:140446458-140446508	MCF-7	breast:	n/a
32	chr9:140444378-140444428	A549	lung:	n/a
33	chr9:140446823-140446873	HEEpiC	esophagus:	n/a
34	chr9:140446240-140446290	Hepatocyte	liver:	n/a
35	chr9:140444966-140445016	NT2-D1	testis:	n/a
36	chr9:140444966-140445016	AG04450	lung:	fetal
37	chr9:140444966-140445016	AG09309	skin:	n/a
38	chr9:140446458-140446508	ECC-1	luminal epithelium:	n/a
39	chr9:140446823-140446873	NHDF-neo	bronchial:	n/a
40	chr9:140444966-140445016	NB4	blood:	n/a
41	chr9:140445760-140445810	PANC-1	pancreas:	n/a
42	chr9:140446823-140446873	HCM	heart:	n/a
43	chr9:140446458-140446508	HCM	heart:	n/a
44	chr9:140446656-140446706	HNPCEpiC	eye:	n/a
45	chr9:140446656-140446706	NHDF-neo	bronchial:	n/a
46	chr9:140446458-140446508	SK-N-SH_RA	brain:	n/a
47	chr9:140444966-140445016	HCPEpiC	choroid plexus:	n/a
48	chr9:140445760-140445810	HNPCEpiC	eye:	n/a
49	chr9:140446993-140447043	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:140446240-140446290	SAEC	small airway:	n/a

(count:37 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 107 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62590220	chr9:140444237-140444238	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs544888536	chr9:140444240-140444241	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs374549311	chr9:140444250-140444251	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs577412868	chr9:140444346-140444347	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs369252626	chr9:140444359-140444360	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs561479383	chr9:140444366-140444367	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs111349825	chr9:140444378-140444379	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs56715636	chr9:140444379-140444380	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540467734	chr9:140444430-140444431	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs559800310	chr9:140444489-140444490	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs528160673	chr9:140444501-140444502	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs34754140	chr9:140444507-140444508	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs149547185	chr9:140444514-140444515	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs570874068	chr9:140444517-140444518	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs530723336	chr9:140444524-140444525	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs182514004	chr9:140444530-140444531	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs147208368	chr9:140444532-140444533	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs536483753	chr9:140444535-140444536	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs369515669	chr9:140444571-140444572	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs370995327	chr9:140444574-140444575	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs372921391	chr9:140444627-140444628	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	rs371394917	chr9:140445584-140445585	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140408600-140444400	Weak transcription	Esophagus	oesophagus
2	chr9:140411200-140444200	Weak transcription	Right Atrium	heart
3	chr9:140429600-140444400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr9:140429800-140444200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:140429800-140444200	Weak transcription	Colon Smooth Muscle	Colon
6	chr9:140429800-140444200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr9:140429800-140444200	Weak transcription	Fetal Lung	lung
8	chr9:140429800-140444200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:140429800-140444600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:140429800-140444600	Weak transcription	NH-A	brain
11	chr9:140431600-140444200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr9:140431600-140444200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:140431800-140444200	Weak transcription	Primary T cells from cord blood	blood
14	chr9:140431800-140444800	Weak transcription	Dnd41	blood
15	chr9:140433000-140444200	Weak transcription	Brain Substantia Nigra	brain
16	chr9:140435400-140444600	Weak transcription	Aorta	Aorta
17	chr9:140437400-140444600	Weak transcription	Fetal Kidney	kidney
18	chr9:140438000-140444200	Weak transcription	Fetal Brain Female	brain
19	chr9:140438400-140444200	Weak transcription	Brain Hippocampus Middle	brain
20	chr9:140439000-140444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr9:140439000-140444200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:140439800-140444400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:140439800-140444400	Weak transcription	HSMM	muscle
24	chr9:140440000-140444200	Weak transcription	HSMMtube	muscle
25	chr9:140440000-140444400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr9:140440400-140444400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:140441200-140444200	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr9:140441200-140444200	Weak transcription	Fetal Intestine Small	intestine
29	chr9:140441400-140444400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:140441600-140444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:140441600-140444200	Weak transcription	Fetal Stomach	stomach
32	chr9:140442000-140444200	Enhancers	Liver	Liver
33	chr9:140442000-140445000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr9:140442200-140444200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr9:140442400-140444200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:140442400-140444400	Weak transcription	Psoas Muscle	Psoas
37	chr9:140442600-140444200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr9:140442800-140444200	Enhancers	Brain Anterior Caudate	brain
39	chr9:140442800-140444200	Weak transcription	Placenta	Placenta
40	chr9:140442800-140444200	Enhancers	Ovary	ovary
41	chr9:140442800-140444200	Weak transcription	HMEC	breast
42	chr9:140442800-140444400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:140442800-140444400	Weak transcription	NHEK	skin
44	chr9:140442800-140444600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr9:140443000-140444200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr9:140443200-140444200	Enhancers	Colonic Mucosa	Colon
47	chr9:140443200-140444400	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr9:140443200-140444800	Enhancers	Spleen	Spleen
49	chr9:140443400-140444200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:140443400-140444200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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