Variant report

Variant	nsv431968
Chromosome Location	chr18:7169248-7264395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:724)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7221435-7221630	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7177250-7177419	HepG2	liver:	n/a	n/a
3	BHLHE40	chr18:7177115-7177352	GM12878	blood:	n/a	n/a
4	BHLHE40	chr18:7202966-7203132	K562	blood:	n/a	chr18:7203078-7203087 chr18:7203078-7203087 chr18:7203072-7203093 chr18:7203077-7203086 chr18:7203076-7203089
5	BRCA1	chr18:7221518-7221712	HepG2	liver:	n/a	n/a
6	BRCA1	chr18:7174539-7174936	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr18:7196717-7197057	IMR90	lung:	n/a	chr18:7196881-7196892
8	CEBPB	chr18:7215652-7215772	HepG2	liver:	n/a	n/a
9	CEBPB	chr18:7173427-7173642	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr18:7200412-7200413	HepG2	liver:	n/a	n/a
11	CEBPB	chr18:7184304-7184596	HepG2	liver:	n/a	n/a
12	CEBPB	chr18:7184351-7184552	A549	lung:	n/a	n/a
13	CEBPB	chr18:7196743-7197013	A549	lung:	n/a	chr18:7196881-7196892
14	CEBPB	chr18:7190660-7190860	HepG2	liver:	n/a	n/a
15	CEBPB	chr18:7174309-7174997	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr18:7199709-7199770	HepG2	liver:	n/a	n/a
17	CEBPB	chr18:7221492-7221783	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr18:7234816-7234956	K562	blood:	n/a	chr18:7234848-7234859 chr18:7234849-7234860
19	CEBPB	chr18:7234687-7235213	HepG2	liver:	n/a	chr18:7234848-7234859 chr18:7234849-7234860
20	CEBPB	chr18:7254364-7254455	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr18:7196707-7197069	HepG2	liver:	n/a	chr18:7196881-7196892
22	CEBPB	chr18:7184425-7184592	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr18:7196803-7196951	H1-hESC	embryonic stem cell:	n/a	chr18:7196881-7196892
24	CEBPB	chr18:7235162-7235245	A549	lung:	n/a	chr18:7235204-7235217
25	CEBPZ	chr18:7177278-7177398	HepG2	liver:	n/a	n/a
26	CHD1	chr18:7177072-7177612	IMR90	lung:	n/a	n/a
27	CHD2	chr18:7174505-7174930	Hela-S3	cervix:	n/a	n/a
28	CTBP2	chr18:7221607-7221929	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr18:7196565-7196642	ProgFib	skin:	n/a	chr18:7196606-7196619 chr18:7196603-7196621
30	CTCF	chr18:7177240-7177390	HPF	lung:	n/a	n/a
31	CTCF	chr18:7196480-7196728	GM12878	blood:	n/a	chr18:7196606-7196619 chr18:7196603-7196621
32	CTCF	chr18:7177240-7177390	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr18:7174740-7174890	HRE	kidney:	n/a	chr18:7174869-7174890 chr18:7174876-7174889
34	CTCF	chr18:7177260-7177410	AG09319	gingival:	n/a	n/a
35	CTCF	chr18:7174718-7175003	K562	blood:	n/a	chr18:7174874-7174892 chr18:7174869-7174890 chr18:7174876-7174889
36	CTCF	chr18:7177121-7177428	HepG2	liver:	n/a	n/a
37	CTCF	chr18:7196520-7196729	MCF-7	breast:	n/a	chr18:7196606-7196619 chr18:7196603-7196621
38	CTCF	chr18:7174809-7174949	K562	blood:	n/a	chr18:7174874-7174892 chr18:7174869-7174890 chr18:7174876-7174889
39	CTCF	chr18:7221420-7221570	A549	lung:	n/a	n/a
40	CTCF	chr18:7177184-7177466	LNCaP	prostate:	n/a	n/a
41	CTCF	chr18:7174763-7174979	Medullo	brain:	n/a	chr18:7174874-7174892 chr18:7174869-7174890 chr18:7174876-7174889
42	CTCF	chr18:7221499-7221707	GM12891	blood:	n/a	n/a
43	CTCF	chr18:7221320-7221470	HAc	cerebellar:	n/a	n/a
44	CTCF	chr18:7221540-7221690	HPF	lung:	n/a	n/a
45	CTCF	chr18:7221520-7221670	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr18:7174740-7174890	HCFaa	heart:	n/a	chr18:7174869-7174890 chr18:7174876-7174889
47	CTCF	chr18:7177240-7177390	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr18:7221488-7221712	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr18:7174776-7174941	K562	blood:	n/a	chr18:7174874-7174892 chr18:7174869-7174890 chr18:7174876-7174889
50	CTCF	chr18:7221500-7221650	SAEC	small airway:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7231086-7231136	AG10803	skin:	n/a
2	chr18:7230489-7230539	HRPEpiC	eye:	n/a
3	chr18:7231534-7231584	HepG2	liver:	n/a
4	chr18:7230245-7230295	Jurkat	blood:	n/a
5	chr18:7231086-7231136	AG04449	skin:	fetal
6	chr18:7230489-7230539	MCF-7	breast:	n/a
7	chr18:7231086-7231136	NH-A	brain:	n/a
8	chr18:7230489-7230539	PANC-1	pancreas:	n/a
9	chr18:7231086-7231136	GM12892	blood:	n/a
10	chr18:7231086-7231136	AG09319	gingival:	n/a
11	chr18:7231534-7231584	HPAEpiC	pulmonary alveolar:	n/a
12	chr18:7229726-7229776	PFSK-1	brain:	n/a
13	chr18:7230245-7230295	HAEpiC	amniotic membrane:	n/a
14	chr18:7229726-7229776	H1-hESC	embryonic stem cell:	embryo
15	chr18:7229726-7229776	PANC-1	pancreas:	n/a
16	chr18:7229726-7229776	NT2-D1	testis:	n/a
17	chr18:7231037-7231087	HCF	heart:	n/a
18	chr18:7230489-7230539	A549	lung:	n/a
19	chr18:7229726-7229776	GM19239	blood:	n/a
20	chr18:7230245-7230295	T-47D	breast:	n/a
21	chr18:7231037-7231087	RPTEC	kidney:	n/a
22	chr18:7229726-7229776	A549	lung:	n/a
23	chr18:7231534-7231584	T-47D	breast:	n/a
24	chr18:7231534-7231584	AoSMC	blood vessel:	n/a
25	chr18:7231086-7231136	IMR90	lung:	fetal
26	chr18:7231086-7231136	Hepatocyte	liver:	n/a
27	chr18:7230489-7230539	AG09319	gingival:	n/a
28	chr18:7231086-7231136	SK-N-SH	brain:	n/a
29	chr18:7229726-7229776	MCF-7	breast:	n/a
30	chr18:7231037-7231087	NT2-D1	testis:	n/a
31	chr18:7231534-7231584	SK-N-SH	brain:	n/a
32	chr18:7230489-7230539	Jurkat	blood:	n/a
33	chr18:7231534-7231584	RPTEC	kidney:	n/a
34	chr18:7231086-7231136	Jurkat	blood:	n/a
35	chr18:7231037-7231087	IMR90	lung:	fetal
36	chr18:7230489-7230539	AoSMC	blood vessel:	n/a
37	chr18:7230245-7230295	HCF	heart:	n/a
38	chr18:7230489-7230539	HCM	heart:	n/a
39	chr18:7231534-7231584	BJ	skin:	n/a
40	chr18:7230245-7230295	NHDF-neo	bronchial:	n/a
41	chr18:7230245-7230295	HRE	kidney:	n/a
42	chr18:7230245-7230295	PrEC	prostate:	n/a
43	chr18:7231534-7231584	HEK293	kidney:	embryo
44	chr18:7230489-7230539	AG04450	lung:	fetal
45	chr18:7229726-7229776	HEK293	kidney:	embryo
46	chr18:7231086-7231136	HUVEC	blood vessel:	n/a
47	chr18:7231086-7231136	HCM	heart:	n/a
48	chr18:7231086-7231136	T-47D	breast:	n/a
49	chr18:7229726-7229776	HRE	kidney:	n/a
50	chr18:7230489-7230539	HCT-116	colon:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:7038272..7039307-chr18:7176844..7177405,3	K562	blood:
2	chr1:117064094..117064942-chr18:7200217..7200777,2	MCF-7	breast:
3	chr18:7251040..7252681-chr18:7255832..7258659,2	K562	blood:
4	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
5	chr18:7037921..7038842-chr18:7174709..7175338,3	MCF-7	breast:
6	chr18:7219560..7222468-chr18:7224893..7227543,2	K562	blood:
7	chr18:7037864..7039267-chr18:7176237..7177839,9	MCF-7	breast:
8	chr18:7237095..7238838-chr18:7283799..7285892,2	K562	blood:
9	chr18:7168069..7170291-chr18:7171310..7174194,2	K562	blood:
10	chr18:7209942..7211874-chr18:7214063..7215628,2	K562	blood:
11	chr18:7022373..7023231-chr18:7176885..7177438,2	MCF-7	breast:
12	chr18:7219560..7222468-chr18:7224893..7227543,2	K562	blood:
13	chr18:7251040..7252681-chr18:7255832..7258659,2	K562	blood:
14	chr18:6920149..6920730-chr18:7177289..7177849,2	K562	blood:
15	chr18:6886014..6886839-chr18:7176913..7177416,2	MCF-7	breast:
16	chr18:7037876..7039021-chr18:7176879..7177788,7	MCF-7	breast:
17	chr18:7209942..7211874-chr18:7214063..7215628,2	K562	blood:
18	chr18:7168069..7170291-chr18:7171310..7174194,2	K562	blood:
19	chr18:6919702..6920513-chr18:7174601..7175401,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-7	chr18:7222430-7222682	l_1518_chr18:7222289-7223722_skeltalMuscle
2	lnc-LAMA1-7	chr18:7222290-7222419	l_1518_chr18:7222289-7223722_skeltalMuscle
3	lnc-LAMA1-7	chr18:7223429-7223722	l_1518_chr18:7222289-7223722_skeltalMuscle

No data

Variant related genes	Relation type
LRRC30	TF binding region
LRRC30	CpG island

Extended variants
information (count: 3717 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3717 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16951343	chr18:7169248-7169249	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10468769	chr18:7169252-7169253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs182071575	chr18:7169259-7169260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs383624	chr18:7169275-7169276	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs150543028	chr18:7169281-7169282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567035179	chr18:7169300-7169301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374449739	chr18:7169303-7169304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539050835	chr18:7169323-7169324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117134299	chr18:7169352-7169353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73380808	chr18:7169377-7169378	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs71807082	chr18:7169407-7169408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs421233	chr18:7169461-7169462	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs139916695	chr18:7169531-7169532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574733925	chr18:7169533-7169534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371412454	chr18:7169575-7169576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199653103	chr18:7169602-7169603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376097425	chr18:7169641-7169642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532286542	chr18:7169643-7169644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73941543	chr18:7169644-7169645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs11416410	chr18:7169665-7169666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs398031928	chr18:7169668-7169669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562361189	chr18:7169716-7169717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73941544	chr18:7169717-7169718	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs455167	chr18:7169723-7169724	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185080196	chr18:7169767-7169768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73380815	chr18:7169775-7169776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs546766016	chr18:7169790-7169791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs446521	chr18:7169792-7169793	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs538979618	chr18:7169829-7169830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76699321	chr18:7169831-7169832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569160795	chr18:7169835-7169836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76417651	chr18:7169842-7169843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555142752	chr18:7169858-7169859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73941545	chr18:7169859-7169860	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534007040	chr18:7169895-7169896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs16951346	chr18:7169896-7169897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576937480	chr18:7169912-7169913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545790309	chr18:7169946-7169947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146728118	chr18:7169971-7169972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs450497	chr18:7169984-7169985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541406474	chr18:7169997-7169998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140369544	chr18:7169998-7169999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565012858	chr18:7170021-7170022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527340613	chr18:7170035-7170036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547054690	chr18:7170059-7170060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560529407	chr18:7170067-7170068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149963185	chr18:7170072-7170073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74896663	chr18:7170089-7170090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs56251931	chr18:7170090-7170091	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs538277147	chr18:7170103-7170104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Heart disease	21282601	CNVD
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
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Breast cancer	17133270	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7163000-7172200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr18:7166000-7169600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr18:7166600-7169600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:7167000-7170200	Weak transcription	Hela-S3	cervix
5	chr18:7167000-7174600	Weak transcription	Spleen	Spleen
6	chr18:7168000-7169800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr18:7168000-7171000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:7168200-7169800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr18:7169000-7173000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr18:7169600-7171600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr18:7169800-7170200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr18:7169800-7170600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr18:7170000-7170200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:7170200-7172600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr18:7170200-7174400	Enhancers	Hela-S3	cervix
16	chr18:7170600-7172600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr18:7171000-7172000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr18:7171600-7172000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:7172000-7172400	Enhancers	Placenta Amnion	Placenta Amnion
20	chr18:7172000-7173000	Enhancers	NH-A	brain
21	chr18:7172000-7173800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr18:7172000-7174000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr18:7172200-7173200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr18:7172400-7173000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr18:7172400-7173000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr18:7172600-7173000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr18:7173000-7173800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr18:7173000-7174400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr18:7173000-7174600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr18:7173200-7173600	Enhancers	Placenta	Placenta
31	chr18:7173800-7175000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr18:7173800-7177000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr18:7174000-7174400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr18:7174400-7174800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr18:7174400-7174800	Flanking Active TSS	Hela-S3	cervix
36	chr18:7174400-7175000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr18:7174400-7175000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr18:7174400-7175200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr18:7174600-7174800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr18:7174600-7175000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr18:7174600-7175000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr18:7174600-7175000	Enhancers	Adipose Nuclei	Adipose
43	chr18:7174600-7175000	Enhancers	Lung	lung
44	chr18:7174600-7175000	Enhancers	Pancreas	Pancrea
45	chr18:7174600-7175200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr18:7174600-7175200	Enhancers	Spleen	Spleen
47	chr18:7174600-7175600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr18:7174800-7175200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr18:7174800-7175400	Enhancers	Hela-S3	cervix
50	chr18:7175000-7176600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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