Variant report

Variant	nsv909357
Chromosome Location	chr18:7524275-7578782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:982)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
3	ARID3A	chr18:7575137-7575406	HepG2	liver:	n/a	n/a
4	ATF2	chr18:7577712-7578133	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr18:7577742-7578206	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
7	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:7542025-7542029	K562	blood:	n/a	n/a
10	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:7575526-7576005	H1-hESC	embryonic stem cell:	n/a	chr18:7575877-7575891
12	BCL11A	chr18:7577811-7577975	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
14	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
15	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
16	BHLHE40	chr18:7575112-7575466	HepG2	liver:	n/a	n/a
17	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
19	CEBPB	chr18:7525858-7525917	HepG2	liver:	n/a	chr18:7525887-7525898
20	CEBPB	chr18:7545933-7546250	A549	lung:	n/a	n/a
21	CEBPB	chr18:7577766-7578084	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr18:7570005-7570017	A549	lung:	n/a	n/a
23	CEBPB	chr18:7577743-7578071	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr18:7545802-7546128	IMR90	lung:	n/a	n/a
25	CEBPB	chr18:7548380-7548578	HepG2	liver:	n/a	n/a
26	CEBPB	chr18:7574543-7574739	A549	lung:	n/a	chr18:7574590-7574603
27	CEBPB	chr18:7576856-7577034	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
32	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
33	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
35	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
36	CHD2	chr18:7577748-7578084	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
38	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
39	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
40	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
42	CREB1	chr18:7568530-7568853	A549	lung:	n/a	n/a
43	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr18:7577760-7578200	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
46	CREB1	chr18:7577860-7578056	A549	lung:	n/a	n/a
47	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr18:7577691-7578228	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
50	CTBP2	chr18:7566540-7567821	H1-hESC	embryonic stem cell:	n/a	n/a

(count:982 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7568186-7568236	HMEC	breast:	n/a
2	chr18:7563847-7563897	PFSK-1	brain:	n/a
3	chr18:7566558-7566608	MCF-7	breast:	n/a
4	chr18:7563847-7563897	U87	brain:	n/a
5	chr18:7566656-7566706	NB4	blood:	n/a
6	chr18:7567638-7567688	K562	blood:	n/a
7	chr18:7568186-7568236	HMEC	breast:	n/a
8	chr18:7563847-7563897	PFSK-1	brain:	n/a
9	chr18:7566558-7566608	MCF-7	breast:	n/a
10	chr18:7563847-7563897	U87	brain:	n/a
11	chr18:7566656-7566706	NB4	blood:	n/a
12	chr18:7567638-7567688	K562	blood:	n/a
13	chr18:7563847-7563897	GM12891	blood:	n/a
14	chr18:7568891-7568941	NT2-D1	testis:	n/a
15	chr18:7567799-7567849	HIPEpiC	eye:	n/a
16	chr18:7567799-7567849	HEEpiC	esophagus:	n/a
17	chr18:7567799-7567849	T-47D	breast:	n/a
18	chr18:7568159-7568209	NH-A	brain:	n/a
19	chr18:7563847-7563897	HRPEpiC	eye:	n/a
20	chr18:7567638-7567688	LNCaP	prostate:	n/a
21	chr18:7567426-7567476	HCF	heart:	n/a
22	chr18:7566258-7566308	AG09319	gingival:	n/a
23	chr18:7568829-7568879	GM12891	blood:	n/a
24	chr18:7567638-7567688	GM12892	blood:	n/a
25	chr18:7563847-7563897	SK-N-SH	brain:	n/a
26	chr18:7567717-7567767	SK-N-MC	brain:	n/a
27	chr18:7567638-7567688	HRPEpiC	eye:	n/a
28	chr18:7567799-7567849	SK-N-MC	brain:	n/a
29	chr18:7568891-7568941	HL-60	blood:	n/a
30	chr18:7566656-7566706	Hepatocyte	liver:	n/a
31	chr18:7567799-7567849	PANC-1	pancreas:	n/a
32	chr18:7568265-7568315	SK-N-SH	brain:	n/a
33	chr18:7566558-7566608	BE2_C	brain:	n/a
34	chr18:7567717-7567767	SKMC	muscle:	n/a
35	chr18:7567426-7567476	HepG2	liver:	n/a
36	chr18:7568539-7568589	HCT-116	colon:	n/a
37	chr18:7568891-7568941	Hepatocyte	liver:	n/a
38	chr18:7567426-7567476	HMEC	breast:	n/a
39	chr18:7568539-7568589	ProgFib	skin:	n/a
40	chr18:7563847-7563897	HEK293	kidney:	embryo
41	chr18:7568265-7568315	HCT-116	colon:	n/a
42	chr18:7568539-7568589	U87	brain:	n/a
43	chr18:7567717-7567767	GM19239	blood:	n/a
44	chr18:7568265-7568315	PFSK-1	brain:	n/a
45	chr18:7566258-7566308	SKMC	muscle:	n/a
46	chr18:7563847-7563897	HAEpiC	amniotic membrane:	n/a
47	chr18:7563847-7563897	ECC-1	luminal epithelium:	n/a
48	chr18:7568159-7568209	SK-N-SH	brain:	n/a
49	chr18:7566258-7566308	GM12891	blood:	n/a
50	chr18:7566781-7566831	GM12878	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:7561940..7563899-chr18:7566456..7568145,3	K562	blood:
2	chr18:7560671..7563899-chr18:7566458..7568145,4	K562	blood:
3	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
4	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
5	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
6	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
7	chr18:7566319..7569036-chr18:7569097..7573393,5	K562	blood:
8	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
9	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
10	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
11	chr18:7560178..7562976-chr18:7564673..7567118,2	MCF-7	breast:

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000149658	chromatin interactions
ENSG00000173482	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs956551	chr18:7524275-7524276	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567744095	chr18:7524280-7524281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536390858	chr18:7524296-7524297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552934952	chr18:7524337-7524338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551938403	chr18:7524357-7524358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566555429	chr18:7524385-7524386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150017568	chr18:7524429-7524430	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558398471	chr18:7524430-7524431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575460627	chr18:7524443-7524444	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs186043565	chr18:7524461-7524462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs555927747	chr18:7524522-7524523	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs554506516	chr18:7524573-7524574	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs574456477	chr18:7524631-7524632	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs78292798	chr18:7524665-7524666	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs74742685	chr18:7524666-7524667	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs571856106	chr18:7524676-7524677	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs549961416	chr18:7524696-7524697	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375026549	chr18:7524697-7524698	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs376507903	chr18:7524823-7524824	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs79973719	chr18:7524905-7524906	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs557480585	chr18:7524992-7524993	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs145233644	chr18:7525012-7525013	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs560308778	chr18:7525014-7525015	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs532110510	chr18:7525108-7525109	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs545823492	chr18:7525131-7525132	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs565526503	chr18:7525165-7525166	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs531155184	chr18:7525232-7525233	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs575963183	chr18:7525236-7525237	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs567798297	chr18:7525240-7525241	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs530112896	chr18:7525257-7525258	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575842741	chr18:7525270-7525271	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs149195240	chr18:7525329-7525330	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs566642309	chr18:7525352-7525353	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs538609917	chr18:7525391-7525392	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs371437760	chr18:7525421-7525422	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192099555	chr18:7525448-7525449	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558686806	chr18:7525456-7525457	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547717730	chr18:7525519-7525520	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs143756300	chr18:7525530-7525531	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs567596590	chr18:7525593-7525594	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs73383666	chr18:7525606-7525607	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs146878388	chr18:7525647-7525648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140744504	chr18:7525719-7525720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534707788	chr18:7525739-7525740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553862533	chr18:7525766-7525767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35048863	chr18:7525776-7525777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556152225	chr18:7525898-7525899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145932744	chr18:7525926-7525927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71870738	chr18:7525927-7525928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576314164	chr18:7525942-7525943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7523200-7525000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr18:7523400-7525000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr18:7523400-7525200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr18:7523400-7525400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:7523600-7525000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr18:7523600-7525600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr18:7523600-7525600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr18:7523600-7525600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr18:7523800-7525000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr18:7523800-7525600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr18:7523800-7525800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr18:7524000-7524400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr18:7524000-7524800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr18:7524000-7524800	Enhancers	HMEC	breast
15	chr18:7524000-7525600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr18:7524200-7524600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr18:7524200-7524600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr18:7524200-7524600	Enhancers	Colon Smooth Muscle	Colon
19	chr18:7524200-7525600	Enhancers	Fetal Thymus	thymus
20	chr18:7524200-7525600	Enhancers	Rectal Smooth Muscle	rectum
21	chr18:7524200-7525800	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr18:7524200-7533000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr18:7524400-7524800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr18:7524400-7525400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:7524600-7525000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr18:7524600-7525200	Flanking Active TSS	Colon Smooth Muscle	Colon
27	chr18:7524600-7525600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr18:7524600-7525600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr18:7524600-7525600	Enhancers	Adipose Nuclei	Adipose
30	chr18:7524800-7525000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr18:7524800-7525600	Active TSS	Stomach Smooth Muscle	stomach
32	chr18:7525000-7525200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr18:7525200-7525400	Enhancers	Colon Smooth Muscle	Colon
34	chr18:7525400-7525600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr18:7525400-7525600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr18:7525600-7525800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr18:7527800-7528000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr18:7527800-7528000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr18:7529000-7529200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr18:7529200-7529400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:7532000-7532400	ZNF genes & repeats	Psoas Muscle	Psoas
42	chr18:7532400-7535800	Weak transcription	Psoas Muscle	Psoas
43	chr18:7533000-7533200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr18:7533000-7533800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr18:7533000-7533800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr18:7533200-7533400	Enhancers	Placenta	Placenta
47	chr18:7533200-7533600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr18:7533400-7533800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr18:7533400-7534400	Weak transcription	Placenta	Placenta
50	chr18:7533600-7533800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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