Variant report

Variant	nsv1004043
Chromosome Location	chr3:80990868-81172472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 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	ARID3A	chr3:81042841-81042940	HepG2	liver:	n/a	n/a
2	BACH1	chr3:81000548-81000921	K562	blood:	n/a	n/a
3	BHLHE40	chr3:81000546-81000924	K562	blood:	n/a	n/a
4	BRCA1	chr3:81000544-81000922	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr3:81000544-81000919	GM12878	blood:	n/a	n/a
6	CEBPB	chr3:81142353-81142605	HepG2	liver:	n/a	chr3:81142507-81142518
7	CEBPB	chr3:81092455-81092788	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:81109072-81109208	H1-hESC	embryonic stem cell:	n/a	chr3:81109165-81109178 chr3:81109167-81109176 chr3:81109165-81109176 chr3:81109167-81109178
9	CEBPB	chr3:81109099-81109299	IMR90	lung:	n/a	chr3:81109165-81109178 chr3:81109167-81109176 chr3:81109165-81109176 chr3:81109167-81109178
10	CEBPB	chr3:81097089-81097614	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:81023476-81023681	A549	lung:	n/a	chr3:81023551-81023562
12	CEBPB	chr3:81023419-81023729	HepG2	liver:	n/a	chr3:81023551-81023562
13	CEBPB	chr3:81034613-81034899	IMR90	lung:	n/a	chr3:81034810-81034821 chr3:81034738-81034749
14	CEBPB	chr3:81023431-81023686	Hela-S3	cervix:	n/a	chr3:81023551-81023562
15	CEBPB	chr3:81082445-81082651	HepG2	liver:	n/a	chr3:81082529-81082540 chr3:81082531-81082540 chr3:81082531-81082540 chr3:81082529-81082542 chr3:81082531-81082540 chr3:81082531-81082540
16	CEBPB	chr3:81023373-81023685	IMR90	lung:	n/a	chr3:81023551-81023562
17	CEBPB	chr3:81034593-81034874	K562	blood:	n/a	chr3:81034810-81034821 chr3:81034738-81034749
18	CEBPB	chr3:81135537-81135787	HepG2	liver:	n/a	chr3:81135678-81135689
19	CEBPB	chr3:81046556-81046862	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:81023419-81023711	K562	blood:	n/a	chr3:81023551-81023562
21	CEBPB	chr3:81109106-81109317	HepG2	liver:	n/a	chr3:81109165-81109178 chr3:81109167-81109176 chr3:81109165-81109176 chr3:81109167-81109178
22	CEBPB	chr3:81034575-81034916	HepG2	liver:	n/a	chr3:81034810-81034821 chr3:81034738-81034749
23	CEBPB	chr3:81142435-81142579	HepG2	liver:	n/a	chr3:81142507-81142518
24	CEBPB	chr3:81000550-81000919	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:81034640-81034832	H1-hESC	embryonic stem cell:	n/a	chr3:81034810-81034821 chr3:81034738-81034749
26	CEBPB	chr3:81034607-81034870	A549	lung:	n/a	chr3:81034810-81034821 chr3:81034738-81034749
27	CEBPB	chr3:81000546-81000922	K562	blood:	n/a	n/a
28	CHD2	chr3:81000544-81000921	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr3:81000546-81000922	K562	blood:	n/a	n/a
30	CTCF	chr3:81055294-81055419	HepG2	liver:	n/a	n/a
31	CTCF	chr3:81055240-81055390	GM12872	blood:	n/a	n/a
32	CTCF	chr3:81055100-81055250	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr3:81055240-81055390	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr3:81055360-81055510	GM12871	blood:	n/a	n/a
35	CTCF	chr3:81055280-81055430	GM12872	blood:	n/a	n/a
36	CTCF	chr3:81029765-81029807	LNCaP	prostate:	n/a	n/a
37	CTCF	chr3:81055220-81055370	GM12871	blood:	n/a	n/a
38	CTCF	chr3:81055255-81055434	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr3:81055260-81055410	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr3:81055248-81055426	GM12878	blood:	n/a	n/a
41	CTCF	chr3:81036723-81036737	GM20000	blood:	n/a	n/a
42	CTCF	chr3:81055300-81055450	GM12869	blood:	n/a	n/a
43	CTCF	chr3:81055260-81055410	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr3:81055171-81055526	GM12878	blood:	n/a	n/a
45	CTCF	chr3:81055340-81055490	BE2_C	brain:	n/a	n/a
46	CTCF	chr3:81055300-81055450	HEK293	kidney:	n/a	n/a
47	CTCF	chr3:81055285-81055395	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr3:81055300-81055450	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr3:81162028-81162085	GM13976	blood:	n/a	n/a
50	CTCF	chr3:81055137-81055424	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:81042167-81042217	NHBE	bronchial:	n/a
2	chr3:81042167-81042217	GM12892	blood:	n/a
3	chr3:81042167-81042217	NB4	blood:	n/a
4	chr3:81042167-81042217	HCM	heart:	n/a
5	chr3:81042167-81042217	AG09309	skin:	n/a
6	chr3:81042167-81042217	HL-60	blood:	n/a
7	chr3:81042167-81042217	AG04449	skin:	fetal
8	chr3:81042167-81042217	HCF	heart:	n/a
9	chr3:81042167-81042217	HIPEpiC	eye:	n/a
10	chr3:81042167-81042217	HCT-116	colon:	n/a
11	chr3:81042167-81042217	ovcar-3	ovarian:	n/a
12	chr3:81042167-81042217	HCPEpiC	choroid plexus:	n/a
13	chr3:81042167-81042217	MCF10A-Er-Src	breast:	n/a
14	chr3:81042167-81042217	HNPCEpiC	eye:	n/a
15	chr3:81042167-81042217	Caco-2	colon:	n/a
16	chr3:81042167-81042217	T-47D	breast:	n/a
17	chr3:81042167-81042217	IMR90	lung:	fetal
18	chr3:81042167-81042217	AG10803	skin:	n/a
19	chr3:81042167-81042217	PANC-1	pancreas:	n/a
20	chr3:81042167-81042217	SKMC	muscle:	n/a
21	chr3:81042167-81042217	GM19239	blood:	n/a
22	chr3:81042167-81042217	SK-N-MC	brain:	n/a
23	chr3:81042167-81042217	SK-N-SH_RA	brain:	n/a
24	chr3:81042167-81042217	AoSMC	blood vessel:	n/a
25	chr3:81042167-81042217	ECC-1	luminal epithelium:	n/a
26	chr3:81042167-81042217	HEEpiC	esophagus:	n/a
27	chr3:81042167-81042217	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:81042167-81042217	HRE	kidney:	n/a
29	chr3:81042167-81042217	BJ	skin:	n/a
30	chr3:81042167-81042217	SAEC	small airway:	n/a
31	chr3:81042167-81042217	Jurkat	blood:	n/a
32	chr3:81042167-81042217	HUVEC	blood vessel:	n/a
33	chr3:81042167-81042217	HEK293	kidney:	embryo
34	chr3:81042167-81042217	NH-A	brain:	n/a
35	chr3:81042167-81042217	AG04450	lung:	fetal
36	chr3:81042167-81042217	ProgFib	skin:	n/a
37	chr3:81042167-81042217	HRCEpiC	kidney:	n/a
38	chr3:81042167-81042217	HMEC	breast:	n/a
39	chr3:81042167-81042217	A549	lung:	n/a
40	chr3:81042167-81042217	HRPEpiC	eye:	n/a
41	chr3:81042167-81042217	GM12891	blood:	n/a
42	chr3:81042167-81042217	GM06990	blood:	n/a
43	chr3:81042167-81042217	PrEC	prostate:	n/a
44	chr3:81042167-81042217	RPTEC	kidney:	n/a
45	chr3:81042167-81042217	CMK	blood:	n/a
46	chr3:81042167-81042217	NT2-D1	testis:	n/a
47	chr3:81042167-81042217	H1-hESC	embryonic stem cell:	embryo
48	chr3:81042167-81042217	BE2_C	brain:	n/a
49	chr3:81042167-81042217	SK-N-SH	brain:	n/a
50	chr3:81042167-81042217	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:81055294..81056046-chr3:81222459..81222973,2	MCF-7	breast:
2	chr3:81054933..81056297-chr3:81222333..81223271,5	MCF-7	breast:
3	chr3:80806849..80809276-chr3:81106708..81109686,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ROBO2-5	chr3:81144263-81144798	XLOC_002717
2	lnc-ROBO2-14	chr3:81072572-81074606	NONHSAT090607
3	lnc-ROBO2-16	chr3:81125669-81125768	l_2399_chr3:81125668-81227822_kidney
4	lnc-ROBO2-14	chr3:81074629-81075472	NONHSAT090607
5	lnc-ROBO2-15	chr3:81076560-81076891	FPKM1_group_21509_transcript_5
6	lnc-ROBO2-15	chr3:81076560-81076891	NONHSAT090608
7	lnc-ROBO2-5	chr3:81043188-81043753	NONHSAT090603
8	lnc-ROBO2-5	chr3:81043009-81043078	NONHSAT090603
9	lnc-ROBO2-5	chr3:81043010-81043078	XLOC_002717
10	lnc-ROBO2-15	chr3:81077747-81077976	NONHSAT090608
11	lnc-ROBO2-5	chr3:81144263-81144462	XLOC_002717
12	lnc-ROBO2-5	chr3:81043034-81043078	XLOC_002717
13	lnc-ROBO2-5	chr3:81144263-81145206	XLOC_002717
14	lnc-ROBO2-5	chr3:81143794-81143915	XLOC_002717
15	lnc-ROBO2-5	chr3:81144263-81146631	XLOC_002717
16	lnc-ROBO2-5	chr3:81043019-81043078	XLOC_002717
17	lnc-ROBO2-5	chr3:81043189-81043753	XLOC_002717
18	lnc-ROBO2-5	chr3:81094515-81094613	XLOC_002717
19	lnc-ROBO2-5	chr3:81143784-81143915	XLOC_002717
20	lnc-ROBO2-5	chr3:81043000-81043078	XLOC_002717
21	lnc-ROBO2-15	chr3:81077747-81077769	FPKM1_group_21509_transcript_5

No data

Variant related genes	Relation type
ENSG00000243694	TF binding region
ENSG00000243694	CpG island
SLC39A10	miRNA target sites
PEG10	miRNA target sites

Extended variants
information (count: 4338 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4338 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187525451	chr3:81020621-81020622	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371224894	chr3:81020624-81020625	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191998328	chr3:81020629-81020630	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374769130	chr3:81020653-81020654	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77175297	chr3:81020690-81020691	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556762437	chr3:81020711-81020712	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548139650	chr3:81020740-81020741	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147745003	chr3:81020743-81020744	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373353942	chr3:81020744-81020745	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555896497	chr3:81020795-81020796	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs28580072	chr3:81020812-81020813	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11716488	chr3:81020819-81020820	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183180001	chr3:81020831-81020832	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs75929941	chr3:81020915-81020916	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs558219951	chr3:81020983-81020984	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs111791556	chr3:81026481-81026482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549233150	chr3:81026482-81026483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559974848	chr3:81026565-81026566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149893048	chr3:81026571-81026572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573807006	chr3:81026601-81026602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370374844	chr3:81026661-81026662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188447317	chr3:81026690-81026691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368026199	chr3:81026768-81026769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531505760	chr3:81026772-81026773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78284800	chr3:81026776-81026777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564182420	chr3:81026836-81026837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527274809	chr3:81026843-81026844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533143516	chr3:81026867-81026868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550293148	chr3:81026941-81026942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200830009	chr3:81026942-81026943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146762663	chr3:81026959-81026960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371871133	chr3:81026996-81026997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535906689	chr3:81027009-81027010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549318954	chr3:81027026-81027027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569425023	chr3:81027032-81027033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117533900	chr3:81027099-81027100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558479954	chr3:81027120-81027121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375254068	chr3:81027129-81027130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571297602	chr3:81027138-81027139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533746466	chr3:81027198-81027199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180873575	chr3:81027205-81027206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148906374	chr3:81027221-81027222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34669609	chr3:81027242-81027243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186522949	chr3:81027277-81027278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190965270	chr3:81027325-81027326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575825469	chr3:81027329-81027330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544939068	chr3:81027339-81027340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564817120	chr3:81027343-81027344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527556690	chr3:81027382-81027383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551782681	chr3:81027397-81027398	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81020600-81020800	Enhancers	Pancreas	Pancrea
2	chr3:81020600-81021000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
3	chr3:81026400-81028000	Enhancers	Brain Germinal Matrix	brain
4	chr3:81026600-81027400	Enhancers	Fetal Brain Female	brain
5	chr3:81026600-81029000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:81027400-81027800	Flanking Active TSS	Fetal Brain Female	brain
7	chr3:81027600-81028200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:81027800-81029200	Weak transcription	Fetal Brain Female	brain
9	chr3:81028200-81028800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:81028600-81029000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:81028800-81029000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr3:81029200-81029400	Enhancers	Fetal Brain Female	brain
13	chr3:81031400-81033600	Enhancers	Fetal Intestine Large	intestine
14	chr3:81031800-81032800	Enhancers	Duodenum Mucosa	Duodenum
15	chr3:81032200-81034000	Enhancers	Fetal Intestine Small	intestine
16	chr3:81041200-81041600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:81041600-81043200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:81042000-81042600	Enhancers	Liver	Liver
19	chr3:81042000-81043000	Enhancers	Fetal Intestine Small	intestine
20	chr3:81042000-81043800	Enhancers	Stomach Mucosa	stomach
21	chr3:81042200-81043000	Enhancers	Fetal Intestine Large	intestine
22	chr3:81042200-81043800	Enhancers	HepG2	liver
23	chr3:81042400-81042800	Enhancers	Duodenum Mucosa	Duodenum
24	chr3:81042600-81043000	Flanking Active TSS	Liver	Liver
25	chr3:81042600-81043200	Enhancers	Small Intestine	intestine
26	chr3:81043000-81044600	Active TSS	Liver	Liver
27	chr3:81043000-81045600	Weak transcription	Fetal Intestine Large	intestine
28	chr3:81043000-81046000	Weak transcription	Fetal Intestine Small	intestine
29	chr3:81043200-81043400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:81043800-81044200	Weak transcription	HepG2	liver
31	chr3:81044200-81044400	Enhancers	HepG2	liver
32	chr3:81044400-81046400	Weak transcription	HepG2	liver
33	chr3:81044600-81045000	Flanking Active TSS	Liver	Liver
34	chr3:81045000-81046200	Enhancers	Liver	Liver
35	chr3:81045600-81048800	Enhancers	Fetal Intestine Large	intestine
36	chr3:81046000-81046200	Enhancers	Fetal Intestine Small	intestine
37	chr3:81046200-81046600	Weak transcription	Fetal Intestine Small	intestine
38	chr3:81046200-81047400	Flanking Active TSS	Liver	Liver
39	chr3:81046400-81047600	Enhancers	HepG2	liver
40	chr3:81046600-81048800	Enhancers	Fetal Intestine Small	intestine
41	chr3:81047400-81049600	Enhancers	Liver	Liver
42	chr3:81048200-81049200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr3:81048600-81049000	Enhancers	Brain Germinal Matrix	brain
44	chr3:81049600-81051600	Weak transcription	Liver	Liver
45	chr3:81051600-81052600	Enhancers	Liver	Liver
46	chr3:81052600-81077800	Weak transcription	Liver	Liver
47	chr3:81077800-81078400	Strong transcription	Liver	Liver
48	chr3:81078400-81094600	Weak transcription	Liver	Liver
49	chr3:81079000-81079200	Enhancers	Fetal Brain Female	brain
50	chr3:81082200-81083000	Enhancers	Pancreatic Islets	Pancreatic Islet

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