Variant report

Variant	nsv1004780
Chromosome Location	chr3:118754727-118820645
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
2	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
3	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
4	CTCF	chr3:118817600-118817750	NB4	blood:	n/a	chr3:118817652-118817670
5	CTCF	chr3:118804080-118804230	MCF-7	breast:	n/a	n/a
6	CTCF	chr3:118817620-118817770	HRPEpiC	eye:	n/a	chr3:118817652-118817670
7	CTCF	chr3:118804080-118804230	A549	lung:	n/a	n/a
8	CTCF	chr3:118804114-118804120	HepG2	liver:	n/a	n/a
9	CTCF	chr3:118817420-118817821	H1-hESC	embryonic stem cell:	n/a	chr3:118817652-118817670
10	CTCF	chr3:118804120-118804270	GM06990	blood:	n/a	n/a
11	CTCF	chr3:118817540-118817690	GM12872	blood:	n/a	chr3:118817652-118817670
12	CTCF	chr3:118817540-118817690	BE2_C	brain:	n/a	chr3:118817652-118817670
13	CTCF	chr3:118804040-118804190	GM12869	blood:	n/a	n/a
14	CTCF	chr3:118817560-118817710	GM12866	blood:	n/a	chr3:118817652-118817670
15	CTCF	chr3:118817540-118817690	NHEK	skin:	n/a	chr3:118817652-118817670
16	CTCF	chr3:118817493-118817804	Medullo	brain:	n/a	chr3:118817652-118817670
17	CTCF	chr3:118817559-118817777	GM13977	blood:	n/a	chr3:118817652-118817670
18	CTCF	chr3:118819300-118819450	HCM	heart:	n/a	n/a
19	CTCF	chr3:118804054-118804152	K562	blood:	n/a	n/a
20	CTCF	chr3:118817580-118817730	AG04449	skin:	n/a	chr3:118817652-118817670
21	CTCF	chr3:118819634-118819725	GM12878	blood:	n/a	n/a
22	CTCF	chr3:118817543-118817794	LNCaP	prostate:	n/a	chr3:118817652-118817670
23	CTCF	chr3:118817580-118817730	GM12865	blood:	n/a	chr3:118817652-118817670
24	CTCF	chr3:118817560-118817710	SAEC	small airway:	n/a	chr3:118817652-118817670
25	CTCF	chr3:118817560-118817710	HFF	foreskin:	n/a	chr3:118817652-118817670
26	CTCF	chr3:118817649-118817710	MCF-7	breast:	n/a	chr3:118817652-118817670
27	CTCF	chr3:118817600-118817750	HEK293	kidney:	n/a	chr3:118817652-118817670
28	CTCF	chr3:118817960-118818110	AG04450	lung:	n/a	n/a
29	CTCF	chr3:118817640-118817790	GM12864	blood:	n/a	chr3:118817652-118817670
30	CTCF	chr3:118804320-118804400	GM10248	blood:	n/a	n/a
31	CTCF	chr3:118817544-118817787	Hela-S3	cervix:	n/a	chr3:118817652-118817670
32	CTCF	chr3:118817580-118817730	GM12873	blood:	n/a	chr3:118817652-118817670
33	CTCF	chr3:118817600-118817750	HBMEC	blood vessel:	n/a	chr3:118817652-118817670
34	CTCF	chr3:118817580-118817730	HRE	kidney:	n/a	chr3:118817652-118817670
35	CTCF	chr3:118817473-118817780	ECC-1	luminal epithelium:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118817559-118817757	GM10266	blood:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118817438-118817834	T-47D	breast:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118817435-118817868	K562	blood:	n/a	chr3:118817652-118817670
39	CTCF	chr3:118817620-118817770	GM12872	blood:	n/a	chr3:118817652-118817670
40	CTCF	chr3:118817580-118817730	AG04450	lung:	n/a	chr3:118817652-118817670
41	CTCF	chr3:118804020-118804170	GM12873	blood:	n/a	n/a
42	CTCF	chr3:118817600-118817750	GM12869	blood:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118817573-118817751	MCF-7	breast:	n/a	chr3:118817652-118817670
44	CTCF	chr3:118803940-118804090	GM12873	blood:	n/a	n/a
45	CTCF	chr3:118817580-118817730	Caco-2	colon:	n/a	chr3:118817652-118817670
46	CTCF	chr3:118817540-118817690	Hela-S3	cervix:	n/a	chr3:118817652-118817670
47	CTCF	chr3:118817580-118817730	HPF	lung:	n/a	chr3:118817652-118817670
48	CTCF	chr3:118817600-118817750	AG10803	skin:	n/a	chr3:118817652-118817670
49	CTCF	chr3:118817466-118817852	HepG2	liver:	n/a	chr3:118817652-118817670
50	CTCF	chr3:118817620-118817770	HUVEC	blood vessel:	n/a	chr3:118817652-118817670

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118757898-118757948	SKMC	muscle:	n/a
2	chr3:118792317-118792367	SAEC	small airway:	n/a
3	chr3:118792317-118792367	MCF-7	breast:	n/a
4	chr3:118792317-118792367	AG10803	skin:	n/a
5	chr3:118792317-118792367	HEEpiC	esophagus:	n/a
6	chr3:118792317-118792367	ovcar-3	ovarian:	n/a
7	chr3:118792317-118792367	HRCEpiC	kidney:	n/a
8	chr3:118757898-118757948	IMR90	lung:	fetal
9	chr3:118757898-118757948	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:118792317-118792367	BE2_C	brain:	n/a
11	chr3:118792317-118792367	SK-N-SH_RA	brain:	n/a
12	chr3:118792317-118792367	HMEC	breast:	n/a
13	chr3:118757898-118757948	HRCEpiC	kidney:	n/a
14	chr3:118792317-118792367	HNPCEpiC	eye:	n/a
15	chr3:118792317-118792367	AG09319	gingival:	n/a
16	chr3:118792317-118792367	HCT-116	colon:	n/a
17	chr3:118792317-118792367	HCPEpiC	choroid plexus:	n/a
18	chr3:118757898-118757948	HCF	heart:	n/a
19	chr3:118757898-118757948	HepG2	liver:	n/a
20	chr3:118792317-118792367	Hela-S3	cervix:	n/a
21	chr3:118757898-118757948	NHDF-neo	bronchial:	n/a
22	chr3:118792317-118792367	RPTEC	kidney:	n/a
23	chr3:118757898-118757948	GM19239	blood:	n/a
24	chr3:118757898-118757948	RPTEC	kidney:	n/a
25	chr3:118792317-118792367	IMR90	lung:	fetal
26	chr3:118792317-118792367	AoSMC	blood vessel:	n/a
27	chr3:118757898-118757948	HMEC	breast:	n/a
28	chr3:118792317-118792367	Jurkat	blood:	n/a
29	chr3:118757898-118757948	HIPEpiC	eye:	n/a
30	chr3:118757898-118757948	AG09319	gingival:	n/a
31	chr3:118792317-118792367	AG09309	skin:	n/a
32	chr3:118757898-118757948	AoSMC	blood vessel:	n/a
33	chr3:118792317-118792367	NB4	blood:	n/a
34	chr3:118757898-118757948	HRPEpiC	eye:	n/a
35	chr3:118792317-118792367	A549	lung:	n/a
36	chr3:118792317-118792367	PANC-1	pancreas:	n/a
37	chr3:118792317-118792367	HL-60	blood:	n/a
38	chr3:118792317-118792367	HEK293	kidney:	embryo
39	chr3:118792317-118792367	GM12878	blood:	n/a
40	chr3:118792317-118792367	HIPEpiC	eye:	n/a
41	chr3:118792317-118792367	HRPEpiC	eye:	n/a
42	chr3:118757898-118757948	HL-60	blood:	n/a
43	chr3:118757898-118757948	A549	lung:	n/a
44	chr3:118757898-118757948	LNCaP	prostate:	n/a
45	chr3:118757898-118757948	HAEpiC	amniotic membrane:	n/a
46	chr3:118757898-118757948	Hela-S3	cervix:	n/a
47	chr3:118757898-118757948	HCM	heart:	n/a
48	chr3:118757898-118757948	SAEC	small airway:	n/a
49	chr3:118757898-118757948	Jurkat	blood:	n/a
50	chr3:118757898-118757948	Caco-2	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
2	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
3	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
4	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
5	chr3:118601491..118603517-chr3:118818904..118820959,2	MCF-7	breast:
6	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
7	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
8	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
9	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
10	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
11	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
12	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
13	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
14	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
15	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
16	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
17	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000144847	chromatin interactions

Extended variants
information (count: 844 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:844 , 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	rs534001678	chr3:118754750-118754751	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs35861	chr3:118754808-118754809	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201105042	chr3:118754881-118754882	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185827569	chr3:118755058-118755059	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537780114	chr3:118755062-118755063	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556028102	chr3:118755104-118755105	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146001583	chr3:118755143-118755144	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76820247	chr3:118755153-118755154	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553451328	chr3:118755257-118755258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572123336	chr3:118755287-118755288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538424425	chr3:118755309-118755310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35862	chr3:118755319-118755320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577498148	chr3:118755327-118755328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544962052	chr3:118755424-118755425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149697619	chr3:118755433-118755434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567384829	chr3:118755469-118755470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs60177242	chr3:118755493-118755494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs62724262	chr3:118755545-118755546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548578503	chr3:118755555-118755556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs59651814	chr3:118755557-118755558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552860192	chr3:118755565-118755566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190252631	chr3:118755584-118755585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148832458	chr3:118755626-118755627	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs552235195	chr3:118755631-118755632	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs35943759	chr3:118755647-118755648	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201090185	chr3:118755735-118755736	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs374703608	chr3:118755775-118755776	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs114684180	chr3:118755800-118755801	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71325356	chr3:118755805-118755806	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs860868	chr3:118755813-118755814	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568027313	chr3:118755846-118755847	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535355607	chr3:118755859-118755860	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114043039	chr3:118755861-118755862	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571926042	chr3:118755866-118755867	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371376004	chr3:118755877-118755878	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76534884	chr3:118755891-118755892	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375304981	chr3:118755923-118755924	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373246611	chr3:118755954-118755955	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375303311	chr3:118755988-118755989	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557877584	chr3:118756045-118756046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145649271	chr3:118756051-118756052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550978478	chr3:118756090-118756091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116215183	chr3:118756142-118756143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180990847	chr3:118756170-118756171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575097729	chr3:118756199-118756200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114595614	chr3:118756285-118756286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560566686	chr3:118756305-118756306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185767296	chr3:118756369-118756370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9840838	chr3:118756402-118756403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs564240230	chr3:118756412-118756413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	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
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118754200-118754800	Bivalent Enhancer	Fetal Thymus	thymus
2	chr3:118754200-118764000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:118754400-118754800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118754400-118754800	Bivalent Enhancer	Thymus	Thymus
5	chr3:118754400-118754800	Enhancers	A549	lung
6	chr3:118754400-118755600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:118754400-118755800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:118754600-118755600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:118754800-118755000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
10	chr3:118755000-118755200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:118755000-118756200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr3:118755000-118756400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr3:118755400-118755600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr3:118755400-118756200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:118755400-118756400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr3:118755600-118755800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr3:118755800-118756000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr3:118755800-118756000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
19	chr3:118758200-118758400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:118761000-118761400	Enhancers	Pancreas	Pancrea
21	chr3:118761200-118761800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr3:118763400-118764400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
23	chr3:118763600-118763800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:118763800-118764400	Active TSS	H9 Cell Line	embryonic stem cell
25	chr3:118763800-118764400	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr3:118763800-118764400	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr3:118763800-118764400	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr3:118764000-118764200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr3:118786800-118787600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:118792200-118792800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr3:118792200-118792800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:118792400-118792800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:118800000-118800400	Enhancers	Brain Germinal Matrix	brain
34	chr3:118803000-118805400	Enhancers	A549	lung
35	chr3:118803400-118804200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr3:118803600-118804000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:118803600-118804000	Enhancers	HMEC	breast
38	chr3:118812000-118812600	Enhancers	A549	lung
39	chr3:118812400-118813000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:118812600-118817400	Weak transcription	A549	lung
41	chr3:118817400-118819400	Enhancers	A549	lung
42	chr3:118818600-118819200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:118819400-118820400	Weak transcription	A549	lung

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