Variant report

Variant	nsv829763
Chromosome Location	chr3:155417552-155470079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:941)
CpG islands
(count:1465)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:155462726-155463100	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:155464514-155465406	HepG2	liver:	n/a	chr3:155464784-155464800
3	ARID3A	chr3:155466486-155467223	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:155463662-155464044	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:155455529-155455971	HepG2	liver:	n/a	n/a
6	ATF2	chr3:155462677-155463122	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:155462570-155463163	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:155463625-155464109	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr3:155462751-155463030	K562	blood:	n/a	n/a
10	BACH1	chr3:155462057-155463080	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:155443204-155443239	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr3:155462357-155463090	K562	blood:	n/a	n/a
13	BHLHE40	chr3:155466806-155467255	HepG2	liver:	n/a	n/a
14	BRCA1	chr3:155462751-155463043	HepG2	liver:	n/a	n/a
15	BRCA1	chr3:155460382-155460383	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:155455717-155455893	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:155462001-155462003	GM12878	blood:	n/a	n/a
18	BRCA1	chr3:155461981-155462170	HepG2	liver:	n/a	n/a
19	CBX3	chr3:155462693-155463129	K562	blood:	n/a	n/a
20	CBX3	chr3:155462719-155463006	K562	blood:	n/a	n/a
21	CCNT2	chr3:155462751-155463179	K562	blood:	n/a	n/a
22	CCNT2	chr3:155461857-155462155	K562	blood:	n/a	chr3:155462028-155462037
23	CEBPB	chr3:155462645-155463227	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:155460355-155460658	K562	blood:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
25	CEBPB	chr3:155433070-155433256	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:155419859-155420206	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:155462962-155463280	K562	blood:	n/a	n/a
28	CEBPB	chr3:155419857-155420223	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:155460352-155460734	K562	blood:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
30	CEBPB	chr3:155432258-155432636	HepG2	liver:	n/a	chr3:155432444-155432457
31	CEBPB	chr3:155432214-155432584	HepG2	liver:	n/a	chr3:155432444-155432457
32	CEBPB	chr3:155460389-155460708	HepG2	liver:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
33	CEBPB	chr3:155419767-155420103	K562	blood:	n/a	n/a
34	CEBPB	chr3:155454437-155454515	K562	blood:	n/a	n/a
35	CEBPB	chr3:155437501-155437764	K562	blood:	n/a	n/a
36	CEBPB	chr3:155432135-155432640	HepG2	liver:	n/a	chr3:155432444-155432457
37	CEBPB	chr3:155460356-155460746	Hela-S3	cervix:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
38	CEBPB	chr3:155456876-155457194	HepG2	liver:	n/a	chr3:155457005-155457018 chr3:155457007-155457018 chr3:155457005-155457016
39	CEBPB	chr3:155460395-155460716	A549	lung:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
40	CEBPB	chr3:155432253-155432619	H1-hESC	embryonic stem cell:	n/a	chr3:155432444-155432457
41	CEBPB	chr3:155432185-155432487	HepG2	liver:	n/a	chr3:155432444-155432457
42	CEBPB	chr3:155462876-155463227	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:155460360-155460721	IMR90	lung:	n/a	chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460530-155460541 chr3:155460532-155460541 chr3:155460532-155460541 chr3:155460532-155460543
44	CEBPD	chr3:155462655-155463101	HepG2	liver:	n/a	n/a
45	CHD2	chr3:155462631-155463156	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr3:155462827-155463121	HepG2	liver:	n/a	n/a
47	CHD2	chr3:155466911-155467208	HepG2	liver:	n/a	n/a
48	CHD2	chr3:155462838-155463003	K562	blood:	n/a	n/a
49	CHD2	chr3:155462074-155462100	HepG2	liver:	n/a	n/a
50	CHD2	chr3:155463601-155464001	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155446146-155446196	HMEC	breast:	n/a
2	chr3:155446146-155446196	HMEC	breast:	n/a
3	chr3:155463780-155463830	PrEC	prostate:	n/a
4	chr3:155446146-155446196	Hepatocyte	liver:	n/a
5	chr3:155422145-155422195	GM12892	blood:	n/a
6	chr3:155462502-155462552	IMR90	lung:	fetal
7	chr3:155463780-155463830	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:155421735-155421785	HRE	kidney:	n/a
9	chr3:155463691-155463741	HL-60	blood:	n/a
10	chr3:155462063-155462113	AG09309	skin:	n/a
11	chr3:155463780-155463830	AG10803	skin:	n/a
12	chr3:155458975-155459025	MCF-7	breast:	n/a
13	chr3:155422103-155422153	ovcar-3	ovarian:	n/a
14	chr3:155422145-155422195	RPTEC	kidney:	n/a
15	chr3:155422103-155422153	IMR90	lung:	fetal
16	chr3:155446146-155446196	H1-hESC	embryonic stem cell:	embryo
17	chr3:155465076-155465126	U87	brain:	n/a
18	chr3:155462425-155462475	Hela-S3	cervix:	n/a
19	chr3:155423168-155423218	HCM	heart:	n/a
20	chr3:155463691-155463741	SK-N-MC	brain:	n/a
21	chr3:155463780-155463830	IMR90	lung:	fetal
22	chr3:155462502-155462552	Hepatocyte	liver:	n/a
23	chr3:155422754-155422804	NHBE	bronchial:	n/a
24	chr3:155422092-155422142	HepG2	liver:	n/a
25	chr3:155462991-155463041	HRCEpiC	kidney:	n/a
26	chr3:155462502-155462552	AG10803	skin:	n/a
27	chr3:155463691-155463741	HCPEpiC	choroid plexus:	n/a
28	chr3:155463133-155463183	HEK293	kidney:	embryo
29	chr3:155463780-155463830	H1-hESC	embryonic stem cell:	embryo
30	chr3:155462063-155462113	Hepatocyte	liver:	n/a
31	chr3:155461845-155461895	HMEC	breast:	n/a
32	chr3:155458975-155459025	HepG2	liver:	n/a
33	chr3:155421735-155421785	AG04450	lung:	fetal
34	chr3:155422145-155422195	HCM	heart:	n/a
35	chr3:155423168-155423218	NB4	blood:	n/a
36	chr3:155463719-155463769	HRPEpiC	eye:	n/a
37	chr3:155463691-155463741	H1-hESC	embryonic stem cell:	embryo
38	chr3:155422129-155422179	GM12891	blood:	n/a
39	chr3:155422092-155422142	GM12892	blood:	n/a
40	chr3:155422129-155422179	Jurkat	blood:	n/a
41	chr3:155462502-155462552	HRCEpiC	kidney:	n/a
42	chr3:155462302-155462352	SKMC	muscle:	n/a
43	chr3:155423168-155423218	BE2_C	brain:	n/a
44	chr3:155446146-155446196	SK-N-SH	brain:	n/a
45	chr3:155422092-155422142	Hela-S3	cervix:	n/a
46	chr3:155462991-155463041	HCM	heart:	n/a
47	chr3:155422971-155423021	HMEC	breast:	n/a
48	chr3:155422103-155422153	H1-hESC	embryonic stem cell:	embryo
49	chr3:155422754-155422804	SK-N-MC	brain:	n/a
50	chr3:155458975-155459025	Caco-2	colon:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:155461079..155463376-chr3:155465033..155467779,3	MCF-7	breast:
2	chr3:155099947..155101105-chr3:155419243..155420372,8	K562	blood:
3	chr3:155449822..155451329-chr3:155456131..155457653,2	K562	blood:
4	chr3:155465236..155465956-chr9:98268514..98269039,2	NB4	blood:
5	chr3:155461486..155465793-chr3:155586998..155592801,6	K562	blood:
6	chr3:155074075..155074622-chr3:155419261..155420274,3	K562	blood:
7	chr3:155099990..155100742-chr3:155420395..155421265,2	MCF-7	breast:
8	chr3:155447543..155449055-chr3:155572391..155574272,2	MCF-7	breast:
9	chr3:155466610..155468263-chr3:155468525..155471754,3	MCF-7	breast:
10	chr3:155420738..155423225-chr3:155424514..155426108,2	MCF-7	breast:
11	chr3:155070467..155071395-chr3:155419423..155420352,4	K562	blood:
12	chr3:155099375..155100930-chr3:155418818..155420546,12	MCF-7	breast:
13	chr3:155460020..155464783-chr3:155465201..155469112,6	K562	blood:
14	chr3:155070527..155071479-chr3:155419274..155420293,4	MCF-7	breast:
15	chr3:155443638..155446622-chr3:155570722..155573140,4	MCF-7	breast:
16	chr3:155100129..155101039-chr3:155419368..155420316,12	MCF-7	breast:
17	chr3:155463358..155465336-chr3:155469536..155471371,2	K562	blood:
18	chr3:155449822..155451329-chr3:155456131..155457653,2	K562	blood:
19	chr3:155406187..155408621-chr3:155417875..155419444,2	K562	blood:
20	chr3:155466610..155468263-chr3:155468525..155471754,3	MCF-7	breast:
21	chr3:155453978..155456582-chr3:155458063..155460908,2	MCF-7	breast:
22	chr3:155459217..155461386-chr3:155623332..155624917,2	K562	blood:
23	chr3:155461931..155462531-chr8:43096224..43096734,2	MCF-7	breast:
24	chr3:155461195..155464539-chr3:155588373..155590107,3	MCF-7	breast:
25	chr3:155463358..155465336-chr3:155469536..155471371,2	K562	blood:
26	chr3:155462054..155464221-chr3:155571081..155573574,2	MCF-7	breast:
27	chr3:155461523..155464397-chr3:155587900..155591398,5	MCF-7	breast:
28	chr3:155461486..155463918-chr3:155586998..155589713,4	K562	blood:
29	chr3:155074208..155074956-chr3:155419567..155420189,2	MCF-7	breast:
30	chr3:155451670..155453673-chr3:155460076..155462927,4	MCF-7	breast:
31	chr3:155462983..155464516-chr3:156391624..156393774,2	MCF-7	breast:
32	chr3:155460891..155464537-chr3:155570941..155574143,3	MCF-7	breast:
33	chr3:155457065..155458861-chr3:155462377..155464396,2	K562	blood:
34	chr3:155461411..155464910-chr3:155465071..155468362,4	MCF-7	breast:
35	chr3:155453978..155456582-chr3:155458063..155460908,2	MCF-7	breast:
36	chr3:155467979..155469957-chr3:155586823..155589749,2	MCF-7	breast:
37	chr3:155138776..155139298-chr3:155419434..155420178,2	MCF-7	breast:
38	chr3:155468097..155470070-chr3:155473602..155476572,2	K562	blood:
39	chr3:155457303..155459109-chr3:155460905..155462872,3	MCF-7	breast:
40	chr3:155072085..155073011-chr3:155419476..155420067,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000214919	TF binding region
PLCH1	TF binding region
ENSG00000214919	CpG island
PLCH1	CpG island
ENSG00000114805	chromatin interactions
ENSG00000163655	chromatin interactions
ENSG00000271155	chromatin interactions
ENSG00000169359	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000214919	chromatin interactions
ENSG00000185920	chromatin interactions
ENSG00000243926	chromatin interactions

Extended variants
information (count: 1894 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13074795	chr3:155417579-155417580	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151187002	chr3:155417611-155417612	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs63545062	chr3:155417612-155417613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181287250	chr3:155417637-155417638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59082626	chr3:155417638-155417639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13095150	chr3:155417649-155417650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139022683	chr3:155417669-155417670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535988407	chr3:155417688-155417689	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538672078	chr3:155417696-155417697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548403652	chr3:155417704-155417705	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569821418	chr3:155417705-155417706	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556767557	chr3:155417711-155417712	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73876921	chr3:155417727-155417728	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149419051	chr3:155417766-155417767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577086267	chr3:155417800-155417801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575328991	chr3:155417836-155417837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117303061	chr3:155417910-155417911	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552967354	chr3:155417938-155417939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574438980	chr3:155417949-155417950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541953864	chr3:155417969-155417970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs358712	chr3:155417971-155417972	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs372019127	chr3:155418012-155418013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554026741	chr3:155418018-155418019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76745597	chr3:155418033-155418034	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs358711	chr3:155418051-155418052	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546010540	chr3:155418071-155418072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573084401	chr3:155418104-155418105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185150064	chr3:155418121-155418122	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540486756	chr3:155418177-155418178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528815952	chr3:155418183-155418184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373558207	chr3:155418202-155418203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562161791	chr3:155418248-155418249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376995441	chr3:155418252-155418253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116615375	chr3:155418279-155418280	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs358710	chr3:155418283-155418284	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs6766660	chr3:155418298-155418299	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs73876923	chr3:155418308-155418309	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552426416	chr3:155418314-155418315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs358709	chr3:155418348-155418349	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189906572	chr3:155418424-155418425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148082093	chr3:155418472-155418473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574327234	chr3:155418540-155418541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs16825322	chr3:155418603-155418604	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs17414810	chr3:155418611-155418612	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561492073	chr3:155418630-155418631	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574925301	chr3:155418642-155418643	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12628990	chr3:155418827-155418828	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545973588	chr3:155418837-155418838	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376482470	chr3:155418891-155418892	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564380528	chr3:155418955-155418956	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155399800-155422000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:155400600-155421000	Weak transcription	Fetal Intestine Small	intestine
3	chr3:155400800-155418400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr3:155408800-155418600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:155409000-155419200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr3:155409000-155419400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:155409200-155418400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:155409200-155422200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr3:155411000-155420600	Weak transcription	Fetal Intestine Large	intestine
10	chr3:155412600-155422400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr3:155412600-155437400	Weak transcription	Pancreas	Pancrea
12	chr3:155413800-155432000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr3:155414000-155418600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:155414000-155420600	Weak transcription	Brain Germinal Matrix	brain
15	chr3:155414800-155419000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr3:155415000-155421200	Weak transcription	Stomach Mucosa	stomach
17	chr3:155415400-155419200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:155415600-155418800	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:155415600-155421400	Weak transcription	Brain Hippocampus Middle	brain
20	chr3:155416400-155418000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:155417400-155421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:155417600-155417800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr3:155417800-155419400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr3:155418000-155421600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:155418400-155418600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:155418400-155420200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:155418600-155419000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr3:155418600-155420200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:155418600-155420200	Enhancers	A549	lung
30	chr3:155418600-155421200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:155418800-155419600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:155418800-155423400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr3:155418800-155423400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:155419000-155419200	Active TSS	Brain Angular Gyrus	brain
35	chr3:155419000-155419600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:155419000-155419800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr3:155419000-155420200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr3:155419200-155419400	Enhancers	Brain Anterior Caudate	brain
39	chr3:155419200-155419600	Enhancers	Rectal Smooth Muscle	rectum
40	chr3:155419200-155419800	Enhancers	Brain Angular Gyrus	brain
41	chr3:155419200-155420400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr3:155419200-155423600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:155419400-155419600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr3:155419400-155419800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:155419400-155419800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:155419400-155419800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:155419400-155419800	Enhancers	Dnd41	blood
48	chr3:155419400-155420200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr3:155419400-155420200	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr3:155419400-155420200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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