Variant report

Variant	esv3364537
Chromosome Location	chr3:140646303-140668571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:140662669-140663315	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140660172-140660863	K562	blood:	n/a	n/a
3	ARID3A	chr3:140660025-140660766	HepG2	liver:	n/a	n/a
4	ATF1	chr3:140660122-140660825	K562	blood:	n/a	n/a
5	ATF2	chr3:140660325-140660781	GM12878	blood:	n/a	chr3:140660559-140660570
6	ATF2	chr3:140660301-140660864	H1-hESC	embryonic stem cell:	n/a	chr3:140660559-140660570
7	ATF2	chr3:140660239-140660875	GM12878	blood:	n/a	chr3:140660559-140660570
8	ATF2	chr3:140659935-140660799	H1-hESC	embryonic stem cell:	n/a	chr3:140660559-140660570
9	ATF3	chr3:140660412-140660829	K562	blood:	n/a	chr3:140660561-140660569 chr3:140660559-140660570 chr3:140660557-140660572 chr3:140660559-140660570 chr3:140660561-140660568 chr3:140660522-140660542 chr3:140660560-140660568 chr3:140660559-140660572 chr3:140660558-140660571
10	BACH1	chr3:140661478-140661701	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:140660138-140660645	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:140659289-140659653	GM12878	blood:	n/a	n/a
13	BCLAF1	chr3:140661073-140661731	GM12878	blood:	n/a	chr3:140661228-140661241
14	BHLHE40	chr3:140660048-140661854	K562	blood:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
15	BHLHE40	chr3:140663088-140663304	HepG2	liver:	n/a	n/a
16	BHLHE40	chr3:140661332-140661868	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:140660346-140660703	A549	lung:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
18	BHLHE40	chr3:140663303-140663344	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:140660098-140660954	HepG2	liver:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
20	BHLHE40	chr3:140663043-140663322	HepG2	liver:	n/a	n/a
21	BHLHE40	chr3:140660259-140660673	HepG2	liver:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
22	BHLHE40	chr3:140660093-140660915	GM12878	blood:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
23	BHLHE40	chr3:140660278-140660702	HepG2	liver:	n/a	chr3:140660527-140660548 chr3:140660531-140660544
24	BRCA1	chr3:140660403-140660833	HepG2	liver:	n/a	n/a
25	BRCA1	chr3:140661368-140662298	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr3:140660105-140660852	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr3:140660373-140660716	GM12878	blood:	n/a	n/a
28	BRCA1	chr3:140660411-140660760	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr3:140659984-140660894	K562	blood:	n/a	n/a
30	CBX3	chr3:140660086-140660804	K562	blood:	n/a	n/a
31	CCNT2	chr3:140660236-140661606	K562	blood:	n/a	chr3:140661234-140661243
32	CEBPB	chr3:140659949-140660731	A549	lung:	n/a	chr3:140660109-140660120
33	CEBPB	chr3:140659930-140660678	K562	blood:	n/a	chr3:140660109-140660120
34	CEBPB	chr3:140650875-140651156	K562	blood:	n/a	n/a
35	CEBPB	chr3:140659953-140660750	HepG2	liver:	n/a	chr3:140660109-140660120
36	CEBPB	chr3:140660425-140660583	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:140660008-140660789	MCF-7	breast:	n/a	chr3:140660109-140660120
38	CEBPB	chr3:140660018-140660246	K562	blood:	n/a	chr3:140660109-140660120
39	CEBPB	chr3:140646209-140646479	K562	blood:	n/a	chr3:140646264-140646276 chr3:140646325-140646336 chr3:140646327-140646338
40	CEBPB	chr3:140659965-140660722	H1-hESC	embryonic stem cell:	n/a	chr3:140660109-140660120
41	CEBPB	chr3:140659934-140660677	IMR90	lung:	n/a	chr3:140660109-140660120
42	CEBPB	chr3:140646162-140646464	Hela-S3	cervix:	n/a	chr3:140646264-140646276 chr3:140646325-140646336 chr3:140646327-140646338
43	CEBPB	chr3:140662006-140662315	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:140646195-140646504	A549	lung:	n/a	chr3:140646264-140646276 chr3:140646325-140646336 chr3:140646327-140646338
45	CEBPB	chr3:140646164-140646519	IMR90	lung:	n/a	chr3:140646264-140646276 chr3:140646325-140646336 chr3:140646327-140646338
46	CEBPB	chr3:140661270-140661753	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:140650826-140651066	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:140659924-140660938	Hela-S3	cervix:	n/a	chr3:140660109-140660120
49	CEBPB	chr3:140646174-140646506	HepG2	liver:	n/a	chr3:140646264-140646276 chr3:140646325-140646336 chr3:140646327-140646338
50	CEBPB	chr3:140659936-140660345	A549	lung:	n/a	chr3:140660109-140660120

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140660432-140660482	HRCEpiC	kidney:	n/a
2	chr3:140660432-140660482	HRCEpiC	kidney:	n/a
3	chr3:140660955-140661005	GM19239	blood:	n/a
4	chr3:140660569-140660619	AoSMC	blood vessel:	n/a
5	chr3:140660569-140660619	SK-N-SH	brain:	n/a
6	chr3:140664727-140664777	SK-N-SH_RA	brain:	n/a
7	chr3:140660748-140660798	SK-N-MC	brain:	n/a
8	chr3:140660955-140661005	GM12891	blood:	n/a
9	chr3:140660335-140660385	AG10803	skin:	n/a
10	chr3:140660457-140660507	NH-A	brain:	n/a
11	chr3:140660457-140660507	HCPEpiC	choroid plexus:	n/a
12	chr3:140660572-140660622	Jurkat	blood:	n/a
13	chr3:140664727-140664777	HEEpiC	esophagus:	n/a
14	chr3:140661733-140661783	Hela-S3	cervix:	n/a
15	chr3:140660569-140660619	GM06990	blood:	n/a
16	chr3:140660748-140660798	HCF	heart:	n/a
17	chr3:140660603-140660653	CMK	blood:	n/a
18	chr3:140660335-140660385	AoSMC	blood vessel:	n/a
19	chr3:140660432-140660482	A549	lung:	n/a
20	chr3:140660432-140660482	GM12891	blood:	n/a
21	chr3:140661601-140661651	LNCaP	prostate:	n/a
22	chr3:140660748-140660798	IMR90	lung:	fetal
23	chr3:140660457-140660507	NB4	blood:	n/a
24	chr3:140660572-140660622	IMR90	lung:	fetal
25	chr3:140660955-140661005	HAEpiC	amniotic membrane:	n/a
26	chr3:140660955-140661005	SKMC	muscle:	n/a
27	chr3:140660642-140660692	LNCaP	prostate:	n/a
28	chr3:140660642-140660692	AoSMC	blood vessel:	n/a
29	chr3:140660572-140660622	HUVEC	blood vessel:	n/a
30	chr3:140664727-140664777	HIPEpiC	eye:	n/a
31	chr3:140660642-140660692	AG04449	skin:	fetal
32	chr3:140660642-140660692	AG09309	skin:	n/a
33	chr3:140660572-140660622	SK-N-MC	brain:	n/a
34	chr3:140660748-140660798	MCF-7	breast:	n/a
35	chr3:140659278-140659328	HIPEpiC	eye:	n/a
36	chr3:140660457-140660507	HNPCEpiC	eye:	n/a
37	chr3:140660569-140660619	AG09309	skin:	n/a
38	chr3:140660603-140660653	HepG2	liver:	n/a
39	chr3:140660642-140660692	HEEpiC	esophagus:	n/a
40	chr3:140660335-140660385	T-47D	breast:	n/a
41	chr3:140661733-140661783	HCF	heart:	n/a
42	chr3:140664727-140664777	A549	lung:	n/a
43	chr3:140660572-140660622	GM12892	blood:	n/a
44	chr3:140660572-140660622	HEK293	kidney:	embryo
45	chr3:140661601-140661651	H1-hESC	embryonic stem cell:	embryo
46	chr3:140660432-140660482	HMEC	breast:	n/a
47	chr3:140660955-140661005	HepG2	liver:	n/a
48	chr3:140661733-140661783	LNCaP	prostate:	n/a
49	chr3:140660569-140660619	HRCEpiC	kidney:	n/a
50	chr3:140661733-140661783	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140660122..140661654-chr3:140682941..140685773,2	K562	blood:
2	chr3:140645222..140647869-chr3:140659939..140662297,3	K562	blood:
3	chr3:140658725..140662722-chr3:140687297..140693458,7	MCF-7	breast:
4	chr3:140657892..140662868-chr3:140689081..140692689,5	MCF-7	breast:
5	chr3:140652670..140656215-chr3:140660256..140665545,6	MCF-7	breast:
6	chr3:140658799..140662032-chr3:140683166..140686698,4	MCF-7	breast:
7	chr3:140642736..140646722-chr3:140659939..140663193,5	K562	blood:
8	chr3:140667358..140669775-chr3:140677233..140679978,2	MCF-7	breast:
9	chr3:140661553..140667904-chr3:140669879..140673651,7	K562	blood:
10	chr3:140645140..140648440-chr3:140656551..140659391,3	K562	blood:
11	chr3:140660106..140661067-chrX:109245318..109246232,2	Hela-S3	cervix:
12	chr3:140641570..140644550-chr3:140649016..140650744,2	K562	blood:
13	chr3:140667610..140670050-chr3:140670451..140673117,3	K562	blood:
14	chr20:52224635..52226312-chr3:140659938..140662134,2	MCF-7	breast:
15	chr17:56707856..56710618-chr3:140659373..140661853,2	MCF-7	breast:
16	chr3:140646297..140647168-chr3:140660373..140660911,2	MCF-7	breast:
17	chr3:140666650..140670047-chr3:140673615..140676647,4	MCF-7	breast:
18	chr3:140666080..140668917-chr3:140671471..140673614,2	MCF-7	breast:
19	chr3:140665869..140666370-chr3:193597000..193597558,2	MCF-7	breast:
20	chr3:140651352..140654120-chr3:140658675..140660598,2	K562	blood:
21	chr3:140659978..140662148-chr3:140682890..140685821,2	MCF-7	breast:
22	chr3:139108349..139110080-chr3:140659758..140661262,2	MCF-7	breast:
23	chr3:140645748..140651447-chr3:140658379..140662815,6	MCF-7	breast:
24	chr3:140651352..140654120-chr3:140658675..140660598,2	K562	blood:
25	chr3:140631695..140633968-chr3:140644648..140646807,2	K562	blood:
26	chr3:140666716..140669469-chr3:140673133..140674994,2	MCF-7	breast:
27	chr3:140645140..140648440-chr3:140656551..140659391,3	K562	blood:
28	chr3:140659978..140660506-chr3:140699204..140700016,2	MCF-7	breast:
29	chr3:140667460..140670151-chr3:140670489..140672455,2	MCF-7	breast:
30	chr3:140659457..140662013-chr3:140675174..140679419,5	K562	blood:
31	chr3:140646965..140650706-chr3:140659494..140663953,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A36-1	chr3:140645814-140646435	l_2485_chr3:140591275-140621447_testes

Variant related genes	Relation type
SLC25A36	TF binding region
SLC25A36	CpG island
ENSG00000212195	chromatin interactions
ENSG00000248773	chromatin interactions
ENSG00000235415	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000157600	chromatin interactions
ENSG00000184432	chromatin interactions
ENSG00000114120	chromatin interactions
ENSG00000248932	chromatin interactions

Extended variants
information (count: 805 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76647961	chr3:140646323-140646324	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs571698499	chr3:140646356-140646357	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs187835517	chr3:140646400-140646401	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs557730256	chr3:140646453-140646454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536153274	chr3:140646459-140646460	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541859346	chr3:140646488-140646489	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555399291	chr3:140646591-140646592	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138026854	chr3:140646619-140646620	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573698469	chr3:140646628-140646629	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs16850915	chr3:140646641-140646642	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs373145907	chr3:140646730-140646731	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192773926	chr3:140646733-140646734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183186060	chr3:140646736-140646737	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143490768	chr3:140646738-140646739	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538201307	chr3:140646756-140646757	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563602366	chr3:140646774-140646775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558174373	chr3:140646813-140646814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145794274	chr3:140646881-140646882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549176052	chr3:140646909-140646910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs578031817	chr3:140646913-140646914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188461907	chr3:140646936-140646937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111246162	chr3:140646992-140646993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528573561	chr3:140647007-140647008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540511471	chr3:140647016-140647017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571655911	chr3:140647050-140647051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539041541	chr3:140647071-140647072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191944416	chr3:140647085-140647086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184737743	chr3:140647096-140647097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189141582	chr3:140647194-140647195	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569558067	chr3:140647228-140647229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536413815	chr3:140647253-140647254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs35552839	chr3:140647282-140647283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11720342	chr3:140647398-140647399	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs370993694	chr3:140647425-140647426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149651067	chr3:140647434-140647435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534410763	chr3:140647463-140647464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144388166	chr3:140647537-140647538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs148784406	chr3:140647574-140647575	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575336394	chr3:140647643-140647644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544626624	chr3:140647656-140647657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563401420	chr3:140647668-140647669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141530429	chr3:140647672-140647673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542581946	chr3:140647686-140647687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573722001	chr3:140647687-140647688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535007155	chr3:140647737-140647738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561131591	chr3:140647764-140647765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545042713	chr3:140647798-140647799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77462538	chr3:140647801-140647802	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112388803	chr3:140647839-140647840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192472995	chr3:140647867-140647868	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	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
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140641600-140646800	Weak transcription	Pancreas	Pancrea
2	chr3:140644000-140646400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:140644200-140646400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:140646400-140646800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:140646400-140646800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:140646400-140647000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:140646600-140646800	Enhancers	HMEC	breast
8	chr3:140646600-140646800	Enhancers	NHEK	skin
9	chr3:140646600-140647000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:140646800-140650200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:140647000-140650000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:140649000-140649200	Enhancers	Pancreas	Pancrea
13	chr3:140649000-140650200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:140649600-140650000	Enhancers	H9 Cell Line	embryonic stem cell
15	chr3:140649600-140650400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:140649600-140650800	Enhancers	HSMM	muscle
17	chr3:140649600-140651400	Enhancers	Muscle Satellite Cultured Cells	--
18	chr3:140649800-140650000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:140649800-140650200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr3:140649800-140650200	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr3:140649800-140650200	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr3:140649800-140650400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:140649800-140650400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:140650000-140650200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr3:140650000-140650200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:140650000-140650200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:140650000-140650200	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr3:140650000-140650200	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr3:140650000-140650200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:140650000-140650400	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr3:140650000-140650400	Active TSS	H9 Cell Line	embryonic stem cell
32	chr3:140650000-140650400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr3:140650000-140650400	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr3:140650000-140650400	Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr3:140650000-140650400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:140650000-140650400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:140650000-140650400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:140650000-140650400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr3:140650000-140650400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:140650000-140650600	Enhancers	Osteobl	bone
41	chr3:140650000-140651000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:140650200-140650400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
43	chr3:140650200-140650400	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr3:140650200-140650400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:140650200-140650400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr3:140650200-140650400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr3:140650200-140650400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr3:140650200-140650400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:140650200-140650600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr3:140650200-140650600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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