Variant report

Variant	esv2757339
Chromosome Location	chr9:71291107-71353743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1320)
CpG islands
(count:489)
Chromatin interactive
region (count:50)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71317436-71317732	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71335807-71336197	K562	blood:	n/a	n/a
3	ARID3A	chr9:71319857-71320037	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:71313920-71314482	K562	blood:	n/a	n/a
5	ARID3A	chr9:71300073-71301012	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:71319020-71319266	K562	blood:	n/a	n/a
7	ARID3A	chr9:71320671-71320784	K562	blood:	n/a	n/a
8	ARID3A	chr9:71321237-71321426	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:71334977-71335149	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:71347230-71347977	HepG2	liver:	n/a	n/a
11	ATF1	chr9:71335758-71336174	K562	blood:	n/a	n/a
12	ATF1	chr9:71314125-71314344	K562	blood:	n/a	n/a
13	ATF2	chr9:71321325-71322566	GM12878	blood:	n/a	n/a
14	ATF2	chr9:71321421-71322309	GM12878	blood:	n/a	n/a
15	ATF3	chr9:71335767-71336300	K562	blood:	n/a	n/a
16	BACH1	chr9:71314082-71314261	K562	blood:	n/a	n/a
17	BACH1	chr9:71320813-71321013	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:71319184-71319411	K562	blood:	n/a	n/a
19	BACH1	chr9:71319599-71320156	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:71317454-71317734	K562	blood:	n/a	n/a
21	BACH1	chr9:71342787-71342894	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr9:71298410-71298619	GM12878	blood:	n/a	chr9:71298514-71298525
23	BATF	chr9:71321805-71322154	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:71321556-71321816	GM12878	blood:	n/a	chr9:71321721-71321730
25	BCL11A	chr9:71321536-71322089	GM12878	blood:	n/a	chr9:71321721-71321730
26	BCL3	chr9:71319918-71320321	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71319925-71319938 chr9:71319926-71319939 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320265-71320278 chr9:71319930-71319939
27	BCL3	chr9:71321460-71322211	GM12878	blood:	n/a	chr9:71321721-71321730
28	BCLAF1	chr9:71321217-71322244	GM12878	blood:	n/a	chr9:71321721-71321730
29	BCLAF1	chr9:71319996-71320510	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320461-71320474 chr9:71320265-71320278
30	BCLAF1	chr9:71321438-71322246	GM12878	blood:	n/a	chr9:71321721-71321730
31	BCLAF1	chr9:71319813-71320483	GM12878	blood:	n/a	chr9:71320125-71320138 chr9:71320133-71320146 chr9:71319925-71319938 chr9:71319926-71319939 chr9:71320127-71320140 chr9:71320211-71320224 chr9:71320141-71320154 chr9:71320461-71320474 chr9:71320265-71320278 chr9:71319930-71319939
32	BHLHE40	chr9:71300694-71300967	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:71346950-71347093	K562	blood:	n/a	n/a
34	BHLHE40	chr9:71323217-71323744	GM12878	blood:	n/a	n/a
35	BHLHE40	chr9:71320803-71321003	GM12878	blood:	n/a	n/a
36	BHLHE40	chr9:71320806-71321476	K562	blood:	n/a	n/a
37	BHLHE40	chr9:71312716-71313047	K562	blood:	n/a	n/a
38	BHLHE40	chr9:71319903-71320790	HepG2	liver:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
39	BHLHE40	chr9:71319893-71320254	GM12878	blood:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
40	BHLHE40	chr9:71319789-71320453	K562	blood:	n/a	chr9:71320130-71320146 chr9:71320133-71320149 chr9:71320214-71320230 chr9:71320125-71320141
41	BHLHE40	chr9:71316803-71316805	K562	blood:	n/a	n/a
42	BHLHE40	chr9:71317542-71317628	K562	blood:	n/a	n/a
43	BHLHE40	chr9:71314074-71314371	K562	blood:	n/a	n/a
44	BHLHE40	chr9:71321464-71322514	GM12878	blood:	n/a	n/a
45	CBX3	chr9:71319837-71320191	K562	blood:	n/a	n/a
46	CCNT2	chr9:71335836-71336116	K562	blood:	n/a	n/a
47	CCNT2	chr9:71319615-71321391	K562	blood:	n/a	chr9:71319903-71319912 chr9:71320696-71320705 chr9:71321382-71321391
48	CCNT2	chr9:71336833-71337075	K562	blood:	n/a	n/a
49	CEBPB	chr9:71335824-71336330	K562	blood:	n/a	chr9:71336134-71336145
50	CEBPB	chr9:71304689-71304980	HepG2	liver:	n/a	chr9:71304821-71304832 chr9:71304821-71304834 chr9:71304823-71304834

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71320693-71320743	GM12892	blood:	n/a
2	chr9:71320693-71320743	GM12892	blood:	n/a
3	chr9:71334425-71334475	HCPEpiC	choroid plexus:	n/a
4	chr9:71334425-71334475	LNCaP	prostate:	n/a
5	chr9:71320671-71320721	SAEC	small airway:	n/a
6	chr9:71320671-71320721	ProgFib	skin:	n/a
7	chr9:71320601-71320651	BJ	skin:	n/a
8	chr9:71320693-71320743	HEEpiC	esophagus:	n/a
9	chr9:71320693-71320743	GM19239	blood:	n/a
10	chr9:71319485-71319535	NHBE	bronchial:	n/a
11	chr9:71319356-71319406	AG10803	skin:	n/a
12	chr9:71319771-71319821	LNCaP	prostate:	n/a
13	chr9:71320693-71320743	ProgFib	skin:	n/a
14	chr9:71319771-71319821	GM19239	blood:	n/a
15	chr9:71319356-71319406	AG04449	skin:	fetal
16	chr9:71319485-71319535	GM12892	blood:	n/a
17	chr9:71334425-71334475	AG09319	gingival:	n/a
18	chr9:71319485-71319535	Hepatocyte	liver:	n/a
19	chr9:71320671-71320721	SK-N-SH	brain:	n/a
20	chr9:71316119-71316169	SK-N-MC	brain:	n/a
21	chr9:71316119-71316169	NB4	blood:	n/a
22	chr9:71320693-71320743	HAEpiC	amniotic membrane:	n/a
23	chr9:71319485-71319535	HUVEC	blood vessel:	n/a
24	chr9:71319771-71319821	T-47D	breast:	n/a
25	chr9:71320601-71320651	SK-N-SH_RA	brain:	n/a
26	chr9:71334425-71334475	AG10803	skin:	n/a
27	chr9:71319356-71319406	LNCaP	prostate:	n/a
28	chr9:71319485-71319535	PFSK-1	brain:	n/a
29	chr9:71319356-71319406	HCM	heart:	n/a
30	chr9:71334425-71334475	IMR90	lung:	fetal
31	chr9:71334425-71334475	NB4	blood:	n/a
32	chr9:71334425-71334475	AG04450	lung:	fetal
33	chr9:71316119-71316169	SKMC	muscle:	n/a
34	chr9:71320671-71320721	AoSMC	blood vessel:	n/a
35	chr9:71319356-71319406	GM12891	blood:	n/a
36	chr9:71319485-71319535	Caco-2	colon:	n/a
37	chr9:71334425-71334475	SK-N-SH	brain:	n/a
38	chr9:71320671-71320721	HCPEpiC	choroid plexus:	n/a
39	chr9:71319771-71319821	H1-hESC	embryonic stem cell:	embryo
40	chr9:71319771-71319821	AoSMC	blood vessel:	n/a
41	chr9:71319356-71319406	HEK293	kidney:	embryo
42	chr9:71319771-71319821	RPTEC	kidney:	n/a
43	chr9:71334425-71334475	Hepatocyte	liver:	n/a
44	chr9:71319356-71319406	AG09309	skin:	n/a
45	chr9:71319485-71319535	HRCEpiC	kidney:	n/a
46	chr9:71320601-71320651	PrEC	prostate:	n/a
47	chr9:71320601-71320651	T-47D	breast:	n/a
48	chr9:71319485-71319535	BJ	skin:	n/a
49	chr9:71334425-71334475	AG09309	skin:	n/a
50	chr9:71319771-71319821	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:71199101..71200031-chr9:71292976..71293754,4	MCF-7	breast:
2	chr9:71310655..71314334-chr9:71315836..71317946,3	K562	blood:
3	chr9:71324675..71326449-chr9:71333129..71335717,2	K562	blood:
4	chr9:71329696..71331473-chr9:71338572..71340155,2	K562	blood:
5	chr9:71329093..71331549-chr9:71334294..71336227,2	K562	blood:
6	chr9:71312864..71316000-chr9:71317726..71321566,4	MCF-7	breast:
7	chr9:71341357..71343787-chr9:71348342..71350761,2	K562	blood:
8	chr9:71317604..71326808-chr9:71328532..71337502,16	K562	blood:
9	chr9:71295770..71299362-chr9:71300231..71303352,3	K562	blood:
10	chr9:71318947..71321633-chr9:71353997..71355633,2	MCF-7	breast:
11	chr9:71320513..71323388-chr9:71323733..71326341,2	MCF-7	breast:
12	chr9:71329093..71331549-chr9:71334294..71336227,2	K562	blood:
13	chr9:71198876..71200125-chr9:71300333..71301861,19	MCF-7	breast:
14	chr9:71318773..71321660-chr9:71357020..71360216,3	K562	blood:
15	chr9:71199112..71200053-chr9:71300525..71301257,2	MCF-7	breast:
16	chr9:71335123..71337478-chr9:71340245..71342058,2	K562	blood:
17	chr9:71316265..71319270-chr9:71393472..71396544,3	MCF-7	breast:
18	chr9:71333196..71335333-chr9:71393276..71395636,2	K562	blood:
19	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
20	chr9:71199401..71199961-chr9:71318970..71319652,2	MCF-7	breast:
21	chr9:71314200..71316006-chr9:71392467..71395218,2	K562	blood:
22	chr9:71318556..71321196-chr9:71331205..71333061,2	MCF-7	breast:
23	chr9:71199033..71199728-chr9:71318176..71318881,4	MCF-7	breast:
24	chr9:71320129..71321713-chr9:71324484..71326376,3	K562	blood:
25	chr9:71319203..71320145-chr9:71614622..71615180,2	MCF-7	breast:
26	chr9:71316561..71319400-chr9:71390897..71393133,2	K562	blood:
27	chr9:71307012..71309934-chr9:71319801..71321541,3	MCF-7	breast:
28	chr9:71313421..71317704-chr9:71318350..71323636,8	K562	blood:
29	chr9:71341357..71343787-chr9:71348342..71350761,2	K562	blood:
30	chr9:71304980..71307129-chr9:71354000..71355533,2	MCF-7	breast:
31	chr9:71317469..71321528-chr9:71322199..71324795,3	MCF-7	breast:
32	chr9:71324675..71326449-chr9:71333129..71335717,2	K562	blood:
33	chr9:71319577..71321555-chr9:71393458..71395334,2	MCF-7	breast:
34	chr9:71198182..71198791-chr9:71300404..71301342,2	MCF-7	breast:
35	chr9:71320241..71323220-chr9:71332885..71336440,3	K562	blood:
36	chr9:71318506..71320929-chr9:71321155..71324459,4	K562	blood:
37	chr9:71310655..71314334-chr9:71315836..71317946,3	K562	blood:
38	chr9:71345141..71347064-chr9:71360683..71362254,2	K562	blood:
39	chr9:71285623..71287326-chr9:71290536..71292237,2	K562	blood:
40	chr9:71208704..71211191-chr9:71318423..71320358,2	MCF-7	breast:
41	chr9:71329696..71331473-chr9:71338572..71340155,2	K562	blood:
42	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
43	chr9:71295770..71299362-chr9:71300231..71303352,3	K562	blood:
44	chr9:71319095..71321406-chr9:71328532..71331423,2	K562	blood:
45	chr9:71335123..71337478-chr9:71340245..71342058,2	K562	blood:
46	chr9:71339890..71342700-chr9:71395822..71397437,2	K562	blood:
47	chr9:71347274..71349362-chr9:71397346..71399719,2	K562	blood:
48	chr9:71317900..71319915-chr9:71391633..71393560,2	K562	blood:
49	chr9:71333441..71335989-chr9:71487302..71489155,2	K562	blood:
50	chr9:71287783..71290645-chr9:71299909..71302251,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM122A-1	chr9:71320902-71321138	NONHSAT131754
2	lnc-FAM122A-1	chr9:71343681-71343850	NONHSAT131753
3	lnc-FAM122A-1	chr9:71342512-71342599	NONHSAT131753
4	lnc-FAM122A-1	chr9:71320901-71321138	NONHSAT131753
5	lnc-FAM122A-1	chr9:71322519-71323057	NONHSAT131754

No data

Variant related genes	Relation type
PIP5K1B	TF binding region
PIP5K1B	CpG island
ENSG00000187866	chromatin interactions
ENSG00000107242	chromatin interactions

Extended variants
information (count: 2127 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2127 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7048378	chr9:71291107-71291108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76428919	chr9:71291108-71291109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189868610	chr9:71291260-71291261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139780539	chr9:71291394-71291395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566782859	chr9:71291396-71291397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534217726	chr9:71291429-71291430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116342382	chr9:71291448-71291449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574136308	chr9:71291462-71291463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544805063	chr9:71291483-71291484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539059207	chr9:71291484-71291485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556265504	chr9:71291514-71291515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183251316	chr9:71291551-71291552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11143394	chr9:71291555-71291556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144728989	chr9:71291581-71291582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187862914	chr9:71291612-71291613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7858883	chr9:71291630-71291631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561272209	chr9:71291644-71291645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531373235	chr9:71291651-71291652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192688939	chr9:71291652-71291653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10869196	chr9:71291727-71291728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533261234	chr9:71291739-71291740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534772063	chr9:71291777-71291778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551502315	chr9:71291804-71291805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566525403	chr9:71291805-71291806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548363620	chr9:71291806-71291807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534232094	chr9:71291860-71291861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555747960	chr9:71291890-71291891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148517627	chr9:71291895-71291896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538007705	chr9:71291910-71291911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185200134	chr9:71291922-71291923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145336847	chr9:71291949-71291950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188435991	chr9:71291966-71291967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192854665	chr9:71291971-71291972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571932356	chr9:71291980-71291981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184777994	chr9:71291987-71291988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560998996	chr9:71292124-71292125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147750242	chr9:71292129-71292130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140985275	chr9:71292147-71292148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75288370	chr9:71292165-71292166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189287626	chr9:71292166-71292167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551440511	chr9:71292194-71292195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560227306	chr9:71292250-71292251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs151287882	chr9:71292257-71292258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374862952	chr9:71292279-71292280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575962174	chr9:71292346-71292347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567822524	chr9:71292358-71292359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538518842	chr9:71292501-71292502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550539787	chr9:71292529-71292530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571845355	chr9:71292538-71292539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76442992	chr9:71292547-71292548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71286800-71293000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:71287400-71293000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:71290400-71291800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:71292000-71294000	Enhancers	Fetal Heart	heart
5	chr9:71292200-71293000	Enhancers	HepG2	liver
6	chr9:71292800-71294000	Enhancers	Primary B cells from peripheral blood	blood
7	chr9:71293000-71293600	Flanking Active TSS	HepG2	liver
8	chr9:71293000-71293800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr9:71293000-71294000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:71293200-71293400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
11	chr9:71293200-71293400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr9:71293200-71293400	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
13	chr9:71293200-71293600	Enhancers	Right Ventricle	heart
14	chr9:71293200-71293800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:71293200-71293800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr9:71293400-71293800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr9:71293400-71293800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
18	chr9:71293600-71293800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:71293600-71293800	Enhancers	HepG2	liver
20	chr9:71294000-71296600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr9:71294000-71298200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:71294000-71298200	Weak transcription	Fetal Heart	heart
23	chr9:71296600-71301000	Enhancers	Primary B cells from peripheral blood	blood
24	chr9:71297200-71301400	Enhancers	Primary B cells from cord blood	blood
25	chr9:71298200-71298600	Enhancers	Fetal Heart	heart
26	chr9:71298200-71298800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:71298200-71298800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr9:71298200-71298800	Enhancers	Stomach Mucosa	stomach
29	chr9:71298200-71299000	Enhancers	Primary hematopoietic stem cells	blood
30	chr9:71298200-71299000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:71298200-71299000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:71298400-71298600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:71298600-71298800	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
34	chr9:71298600-71303200	Weak transcription	Fetal Heart	heart
35	chr9:71298800-71299200	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr9:71298800-71300200	Weak transcription	Stomach Mucosa	stomach
37	chr9:71298800-71303400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:71299800-71300400	Enhancers	HepG2	liver
39	chr9:71300200-71300600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr9:71300200-71300600	Enhancers	Stomach Mucosa	stomach
41	chr9:71300400-71300800	Flanking Active TSS	HepG2	liver
42	chr9:71300600-71300800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:71300600-71304000	Weak transcription	Stomach Mucosa	stomach
44	chr9:71300800-71301000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr9:71300800-71301000	Enhancers	HepG2	liver
46	chr9:71303200-71308400	Enhancers	Fetal Heart	heart
47	chr9:71303400-71306800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:71303800-71306600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr9:71304000-71304200	Enhancers	Left Ventricle	heart
50	chr9:71304000-71304400	Enhancers	Stomach Mucosa	stomach

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