Variant report

Variant	nsv520047
Chromosome Location	chr5:101541784-101566107
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	chr5:101559542-101559874	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:101551961-101552911	HepG2	liver:	n/a	chr5:101552035-101552051
3	ARID3A	chr5:101558223-101559288	HepG2	liver:	n/a	n/a
4	BATF	chr5:101553848-101554117	GM12878	blood:	n/a	chr5:101553951-101553960
5	BHLHE40	chr5:101553984-101554248	HepG2	liver:	n/a	n/a
6	BHLHE40	chr5:101558455-101558904	HepG2	liver:	n/a	n/a
7	BHLHE40	chr5:101558583-101558831	HepG2	liver:	n/a	n/a
8	BRCA1	chr5:101559586-101559705	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:101546929-101547277	HepG2	liver:	n/a	chr5:101547099-101547110 chr5:101547084-101547095
10	CEBPB	chr5:101558531-101558886	HepG2	liver:	n/a	chr5:101558770-101558781 chr5:101558772-101558783
11	CEBPB	chr5:101552558-101552836	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:101558532-101558922	HepG2	liver:	n/a	chr5:101558770-101558781 chr5:101558772-101558783
13	CEBPB	chr5:101558645-101559090	A549	lung:	n/a	chr5:101558770-101558781 chr5:101559037-101559050 chr5:101559039-101559050 chr5:101558772-101558783
14	CEBPB	chr5:101558524-101558873	HepG2	liver:	n/a	chr5:101558770-101558781 chr5:101558772-101558783
15	CEBPB	chr5:101558191-101559059	MCF-7	breast:	n/a	chr5:101558770-101558781 chr5:101559037-101559050 chr5:101559039-101559050 chr5:101558772-101558783
16	CEBPB	chr5:101558556-101558984	MCF-7	breast:	n/a	chr5:101558770-101558781 chr5:101558772-101558783
17	CEBPB	chr5:101552538-101552742	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:101558486-101559039	HepG2	liver:	n/a	chr5:101558770-101558781 chr5:101558772-101558783
19	CEBPD	chr5:101558600-101558854	HepG2	liver:	n/a	n/a
20	CTCF	chr5:101559620-101559770	Caco-2	colon:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
21	CTCF	chr5:101559720-101559870	GM06990	blood:	n/a	n/a
22	CTCF	chr5:101559640-101559790	HA-sp	spinal cord:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
23	CTCF	chr5:101559660-101559810	HEEpiC	esophagus:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
24	CTCF	chr5:101559575-101559867	Medullo	brain:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
25	CTCF	chr5:101559540-101559690	AG04450	lung:	n/a	n/a
26	CTCF	chr5:101559620-101559770	GM12871	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
27	CTCF	chr5:101559620-101559770	K562	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
28	CTCF	chr5:101559660-101559810	SK-N-SH_RA	brain:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
29	CTCF	chr5:101559573-101559803	SK-N-SH_RA	brain:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
30	CTCF	chr5:101559546-101559975	SK-N-SH	brain:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
31	CTCF	chr5:101559645-101559812	GM13976	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
32	CTCF	chr5:101559640-101559790	HRE	kidney:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
33	CTCF	chr5:101559619-101559849	Pancreas_OC	pancreas:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
34	CTCF	chr5:101559640-101559790	HL-60	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
35	CTCF	chr5:101559567-101559869	A549	lung:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
36	CTCF	chr5:101559600-101559750	GM12868	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
37	CTCF	chr5:101559580-101559730	NHEK	skin:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
38	CTCF	chr5:101559600-101559750	HVMF	connective:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
39	CTCF	chr5:101559520-101559670	HAc	cerebellar:	n/a	n/a
40	CTCF	chr5:101559660-101559810	HFF-Myc	foreskin:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
41	CTCF	chr5:101559629-101559832	GM10248	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
42	CTCF	chr5:101559660-101559810	NHDF-neo	bronchial:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
43	CTCF	chr5:101559640-101559790	HMEC	breast:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
44	CTCF	chr5:101559640-101559790	AG04450	lung:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
45	CTCF	chr5:101559600-101559750	NHDF-neo	bronchial:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
46	CTCF	chr5:101559640-101559790	RPTEC	kidney:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
47	CTCF	chr5:101559660-101559796	GM20000	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
48	CTCF	chr5:101559640-101559790	AG10803	skin:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
49	CTCF	chr5:101559660-101559810	WERI-Rb-1	eye:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726
50	CTCF	chr5:101559680-101559830	GM12872	blood:	n/a	chr5:101559706-101559727 chr5:101559711-101559729 chr5:101559713-101559726

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101552551-101552601	SK-N-SH_RA	brain:	n/a
2	chr5:101552551-101552601	SK-N-SH_RA	brain:	n/a
3	chr5:101552551-101552601	HUVEC	blood vessel:	n/a
4	chr5:101552551-101552601	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:101552551-101552601	A549	lung:	n/a
6	chr5:101552551-101552601	HL-60	blood:	n/a
7	chr5:101552551-101552601	HCPEpiC	choroid plexus:	n/a
8	chr5:101552551-101552601	AG09319	gingival:	n/a
9	chr5:101552551-101552601	SKMC	muscle:	n/a
10	chr5:101552551-101552601	HIPEpiC	eye:	n/a
11	chr5:101552551-101552601	GM19239	blood:	n/a
12	chr5:101552551-101552601	AG10803	skin:	n/a
13	chr5:101552551-101552601	HEEpiC	esophagus:	n/a
14	chr5:101552551-101552601	ProgFib	skin:	n/a
15	chr5:101552551-101552601	HRPEpiC	eye:	n/a
16	chr5:101552551-101552601	HCM	heart:	n/a
17	chr5:101552551-101552601	NH-A	brain:	n/a
18	chr5:101552551-101552601	H1-hESC	embryonic stem cell:	embryo
19	chr5:101552551-101552601	GM06990	blood:	n/a
20	chr5:101552551-101552601	HAEpiC	amniotic membrane:	n/a
21	chr5:101552551-101552601	AG04449	skin:	fetal
22	chr5:101552551-101552601	RPTEC	kidney:	n/a
23	chr5:101552551-101552601	NT2-D1	testis:	n/a
24	chr5:101552551-101552601	HMEC	breast:	n/a
25	chr5:101552551-101552601	Jurkat	blood:	n/a
26	chr5:101552551-101552601	IMR90	lung:	fetal
27	chr5:101552551-101552601	HEK293	kidney:	embryo
28	chr5:101552551-101552601	K562	blood:	n/a
29	chr5:101552551-101552601	CMK	blood:	n/a
30	chr5:101552551-101552601	SK-N-MC	brain:	n/a
31	chr5:101552551-101552601	HRCEpiC	kidney:	n/a
32	chr5:101552551-101552601	BJ	skin:	n/a
33	chr5:101552551-101552601	MCF-7	breast:	n/a
34	chr5:101552551-101552601	PFSK-1	brain:	n/a
35	chr5:101552551-101552601	GM12891	blood:	n/a
36	chr5:101552551-101552601	NHDF-neo	bronchial:	n/a
37	chr5:101552551-101552601	NHBE	bronchial:	n/a
38	chr5:101552551-101552601	PrEC	prostate:	n/a
39	chr5:101552551-101552601	HNPCEpiC	eye:	n/a
40	chr5:101552551-101552601	Caco-2	colon:	n/a
41	chr5:101552551-101552601	AG04450	lung:	fetal
42	chr5:101552551-101552601	AoSMC	blood vessel:	n/a
43	chr5:101552551-101552601	U87	brain:	n/a
44	chr5:101552551-101552601	BE2_C	brain:	n/a
45	chr5:101552551-101552601	HRE	kidney:	n/a
46	chr5:101552551-101552601	HCT-116	colon:	n/a
47	chr5:101552551-101552601	HCF	heart:	n/a
48	chr5:101552551-101552601	PANC-1	pancreas:	n/a
49	chr5:101552551-101552601	ECC-1	luminal epithelium:	n/a
50	chr5:101552551-101552601	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:98439759..98440660-chr5:101559209..101559794,3	K562	blood:

Variant related genes	Relation type
ENSG00000268424	TF binding region
ENSG00000268424	CpG island

Extended variants
information (count: 708 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566389845	chr5:101546442-101546443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539627798	chr5:101546496-101546497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558370646	chr5:101546503-101546504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115015840	chr5:101546519-101546520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188307463	chr5:101546608-101546609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4703214	chr5:101546639-101546640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148964576	chr5:101546646-101546647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541301941	chr5:101546716-101546717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533862897	chr5:101546729-101546730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559366616	chr5:101546749-101546750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192197233	chr5:101546763-101546764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs60420300	chr5:101546821-101546822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs13187810	chr5:101546822-101546823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553634650	chr5:101546823-101546824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530475931	chr5:101546828-101546829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553894757	chr5:101546847-101546848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13187963	chr5:101546888-101546889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548679512	chr5:101546910-101546911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13187989	chr5:101546936-101546937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560515177	chr5:101546939-101546940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528054235	chr5:101546958-101546959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200859422	chr5:101546994-101546995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546608382	chr5:101547009-101547010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566233286	chr5:101547030-101547031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570691782	chr5:101547066-101547067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144259987	chr5:101547067-101547068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565671809	chr5:101547069-101547070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73183710	chr5:101547073-101547074	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553231928	chr5:101547083-101547084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146733778	chr5:101547089-101547090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114061531	chr5:101547129-101547130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183877895	chr5:101547154-101547155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201227867	chr5:101547216-101547217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182032200	chr5:101547217-101547218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146482499	chr5:101547218-101547219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138851176	chr5:101547231-101547232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553375974	chr5:101547235-101547236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140318599	chr5:101547248-101547249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576249256	chr5:101547290-101547291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545291287	chr5:101547300-101547301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543319781	chr5:101547331-101547332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556837360	chr5:101547332-101547333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575113278	chr5:101547355-101547356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78353893	chr5:101547449-101547450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184521341	chr5:101547485-101547486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191703851	chr5:101547500-101547501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528211020	chr5:101547648-101547649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145437626	chr5:101547670-101547671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138166270	chr5:101547671-101547672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200193778	chr5:101547689-101547690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101546400-101547800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:101546400-101547800	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr5:101546800-101547200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr5:101546800-101547400	Enhancers	HepG2	liver
5	chr5:101546800-101547600	Enhancers	Liver	Liver
6	chr5:101547200-101548200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr5:101547400-101551800	Weak transcription	HepG2	liver
8	chr5:101547600-101551800	Weak transcription	Liver	Liver
9	chr5:101548200-101548400	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:101549400-101549600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr5:101550600-101551200	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr5:101551200-101551800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:101551400-101551800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:101551800-101552000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr5:101551800-101552000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr5:101551800-101552000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr5:101551800-101552000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:101551800-101552000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr5:101551800-101552200	Enhancers	Liver	Liver
20	chr5:101551800-101552400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:101551800-101553000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:101551800-101553200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:101551800-101553200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:101551800-101553400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:101551800-101555000	Enhancers	HepG2	liver
26	chr5:101552000-101552200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr5:101552000-101552400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:101552000-101552400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:101552000-101553200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr5:101552200-101552600	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr5:101552200-101552600	Flanking Active TSS	Liver	Liver
32	chr5:101552200-101553200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr5:101552400-101552600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:101552400-101553400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr5:101552600-101552800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr5:101552600-101552800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr5:101552600-101553200	Enhancers	Liver	Liver
38	chr5:101553200-101553400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:101553200-101553600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
40	chr5:101553200-101553600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
41	chr5:101553200-101554000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr5:101553200-101554000	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr5:101553200-101554400	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr5:101553400-101553600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:101553400-101553600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr5:101553400-101553800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr5:101553800-101554000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:101555000-101555400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:101557400-101558200	ZNF genes & repeats	Liver	Liver
50	chr5:101557400-101558400	ZNF genes & repeats	HepG2	liver

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