Variant report

Variant	nsv882715
Chromosome Location	chr5:111836278-111894491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:854)
CpG islands
(count:62)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:111883792-111884704	K562	blood:	n/a	n/a
2	ARID3A	chr5:111885471-111885834	K562	blood:	n/a	n/a
3	ARID3A	chr5:111887108-111887506	HepG2	liver:	n/a	n/a
4	ATF1	chr5:111885435-111885835	K562	blood:	n/a	n/a
5	ATF1	chr5:111887067-111887475	K562	blood:	n/a	n/a
6	ATF1	chr5:111883809-111884514	K562	blood:	n/a	n/a
7	ATF2	chr5:111859505-111859944	GM12878	blood:	n/a	n/a
8	ATF2	chr5:111858477-111858860	GM12878	blood:	n/a	n/a
9	ATF3	chr5:111883905-111884341	K562	blood:	n/a	n/a
10	BACH1	chr5:111883993-111884306	K562	blood:	n/a	n/a
11	BACH1	chr5:111881564-111881599	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:111859586-111859905	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:111858657-111858905	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:111859579-111859851	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:111859567-111859912	GM12878	blood:	n/a	n/a
16	BCL3	chr5:111889621-111889915	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:111859495-111859911	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:111883012-111884569	K562	blood:	n/a	n/a
19	BHLHE40	chr5:111856274-111856499	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:111871142-111871394	K562	blood:	n/a	n/a
21	BHLHE40	chr5:111887261-111887419	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:111886978-111887474	K562	blood:	n/a	n/a
23	BHLHE40	chr5:111849758-111850131	K562	blood:	n/a	n/a
24	BHLHE40	chr5:111859597-111859824	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:111887168-111887529	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr5:111883807-111884530	K562	blood:	n/a	n/a
27	CBX3	chr5:111848011-111848313	K562	blood:	n/a	n/a
28	CBX3	chr5:111883876-111884412	K562	blood:	n/a	n/a
29	CCNT2	chr5:111883510-111884478	K562	blood:	n/a	n/a
30	CCNT2	chr5:111885389-111886039	K562	blood:	n/a	n/a
31	CEBPB	chr5:111880802-111881062	A549	lung:	n/a	chr5:111880925-111880936
32	CEBPB	chr5:111851217-111851405	IMR90	lung:	n/a	chr5:111851295-111851306
33	CEBPB	chr5:111851157-111851483	K562	blood:	n/a	chr5:111851295-111851306
34	CEBPB	chr5:111880760-111881072	K562	blood:	n/a	chr5:111880925-111880936
35	CEBPB	chr5:111883825-111884459	K562	blood:	n/a	n/a
36	CEBPB	chr5:111883731-111884316	K562	blood:	n/a	n/a
37	CEBPB	chr5:111865341-111865496	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:111851175-111851485	HepG2	liver:	n/a	chr5:111851295-111851306
39	CEBPB	chr5:111880780-111881054	HepG2	liver:	n/a	chr5:111880925-111880936
40	CEBPB	chr5:111851214-111851467	A549	lung:	n/a	chr5:111851295-111851306
41	CEBPB	chr5:111880784-111881051	IMR90	lung:	n/a	chr5:111880925-111880936
42	CEBPD	chr5:111885322-111885980	K562	blood:	n/a	n/a
43	CEBPD	chr5:111885411-111885943	K562	blood:	n/a	n/a
44	CEBPD	chr5:111883761-111884482	K562	blood:	n/a	n/a
45	CEBPD	chr5:111883757-111884404	K562	blood:	n/a	n/a
46	CHD1	chr5:111858696-111858722	GM12878	blood:	n/a	n/a
47	CHD2	chr5:111859254-111859889	GM12878	blood:	n/a	n/a
48	CHD2	chr5:111858540-111858992	GM12878	blood:	n/a	n/a
49	CTCF	chr5:111886920-111887070	GM06990	blood:	n/a	n/a
50	CTCF	chr5:111865400-111865550	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:111869581-111869631	HEK293	kidney:	embryo
2	chr5:111869581-111869631	HEK293	kidney:	embryo
3	chr5:111869581-111869631	MCF-7	breast:	n/a
4	chr5:111869581-111869631	HAEpiC	amniotic membrane:	n/a
5	chr5:111869581-111869631	RPTEC	kidney:	n/a
6	chr5:111869581-111869631	ovcar-3	ovarian:	n/a
7	chr5:111869581-111869631	GM12891	blood:	n/a
8	chr5:111869581-111869631	PFSK-1	brain:	n/a
9	chr5:111869581-111869631	AG04450	lung:	fetal
10	chr5:111869581-111869631	NH-A	brain:	n/a
11	chr5:111869581-111869631	HRE	kidney:	n/a
12	chr5:111869581-111869631	SK-N-SH_RA	brain:	n/a
13	chr5:111869581-111869631	IMR90	lung:	fetal
14	chr5:111869581-111869631	U87	brain:	n/a
15	chr5:111869581-111869631	GM12892	blood:	n/a
16	chr5:111869581-111869631	SAEC	small airway:	n/a
17	chr5:111869581-111869631	NHDF-neo	bronchial:	n/a
18	chr5:111869581-111869631	Jurkat	blood:	n/a
19	chr5:111869581-111869631	HEEpiC	esophagus:	n/a
20	chr5:111869581-111869631	PrEC	prostate:	n/a
21	chr5:111869581-111869631	GM12878	blood:	n/a
22	chr5:111869581-111869631	ProgFib	skin:	n/a
23	chr5:111869581-111869631	PANC-1	pancreas:	n/a
24	chr5:111869581-111869631	NT2-D1	testis:	n/a
25	chr5:111869581-111869631	NB4	blood:	n/a
26	chr5:111869581-111869631	HUVEC	blood vessel:	n/a
27	chr5:111869581-111869631	HCT-116	colon:	n/a
28	chr5:111869581-111869631	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:111869581-111869631	HCM	heart:	n/a
30	chr5:111869581-111869631	HRCEpiC	kidney:	n/a
31	chr5:111869581-111869631	HCF	heart:	n/a
32	chr5:111869581-111869631	AG04449	skin:	fetal
33	chr5:111869581-111869631	HMEC	breast:	n/a
34	chr5:111869581-111869631	LNCaP	prostate:	n/a
35	chr5:111869581-111869631	A549	lung:	n/a
36	chr5:111869581-111869631	SKMC	muscle:	n/a
37	chr5:111869581-111869631	HepG2	liver:	n/a
38	chr5:111869581-111869631	AG09319	gingival:	n/a
39	chr5:111869581-111869631	NHBE	bronchial:	n/a
40	chr5:111869581-111869631	MCF10A-Er-Src	breast:	n/a
41	chr5:111869581-111869631	Hepatocyte	liver:	n/a
42	chr5:111869581-111869631	AoSMC	blood vessel:	n/a
43	chr5:111869581-111869631	ECC-1	luminal epithelium:	n/a
44	chr5:111869581-111869631	GM19239	blood:	n/a
45	chr5:111869581-111869631	AG09309	skin:	n/a
46	chr5:111869581-111869631	K562	blood:	n/a
47	chr5:111869581-111869631	BE2_C	brain:	n/a
48	chr5:111869581-111869631	HCPEpiC	choroid plexus:	n/a
49	chr5:111869581-111869631	GM06990	blood:	n/a
50	chr5:111869581-111869631	HL-60	blood:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr5:111886306..111888838-chr5:111889426..111891005,2	K562	blood:
2	chr5:111857753..111860186-chr5:111861145..111863385,2	K562	blood:
3	chr5:111827820..111828819-chr5:111886665..111887192,2	MCF-7	breast:
4	chr5:111835502..111837243-chr5:111837890..111840358,2	MCF-7	breast:
5	chr5:111886884..111887988-chr5:111940509..111941323,3	K562	blood:
6	chr5:111886837..111887799-chr5:112092992..112093906,9	K562	blood:
7	chr3:124140032..124140554-chr5:111855676..111856423,2	MCF-7	breast:
8	chr5:111886856..111887404-chr5:112046425..112047135,2	MCF-7	breast:
9	chr5:111868244..111870833-chr5:111871300..111873976,2	K562	blood:
10	chr5:111884694..111888064-chr5:112042220..112044384,3	MCF-7	breast:
11	chr5:111827330..111830310-chr5:111838037..111840196,2	MCF-7	breast:
12	chr5:111886846..111887851-chr5:112092877..112093891,4	MCF-7	breast:
13	chr5:111868244..111870833-chr5:111871300..111873976,2	K562	blood:
14	chr5:111887607..111889700-chr5:111892241..111894417,2	K562	blood:
15	chr5:111881836..111883481-chr5:112041986..112044748,2	K562	blood:
16	chr5:111887607..111889700-chr5:111892241..111894417,2	K562	blood:
17	chr5:111871115..111873160-chr5:111927827..111929771,2	K562	blood:
18	chr5:111887498..111890102-chr5:112044744..112046649,2	MCF-7	breast:
19	chr5:111886306..111888838-chr5:111889426..111891005,2	K562	blood:
20	chr2:150164278..150165118-chr5:111885955..111886738,2	MCF-7	breast:
21	chr5:111868244..111870833-chr5:111871300..111873976,3	K562	blood:
22	chr5:111857753..111860186-chr5:111861145..111863385,2	K562	blood:
23	chr5:111868244..111870833-chr5:111871300..111873976,3	K562	blood:
24	chr5:111496398..111498686-chr5:111868058..111870036,2	MCF-7	breast:
25	chr5:111835502..111837243-chr5:111837890..111840358,2	MCF-7	breast:
26	chr5:111827723..111828709-chr5:111886769..111887504,3	MCF-7	breast:
27	chr5:111496580..111499144-chr5:111884789..111886840,2	K562	blood:
28	chr5:111887102..111888171-chr5:112026844..112028152,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APC-7	chr5:111882670-111883202	NONHSAT103231

No data

Variant related genes	Relation type
ENSG00000251014	TF binding region
ENSG00000251014	CpG island
ENSG00000224032	chromatin interactions
ENSG00000238363	chromatin interactions
ENSG00000134982	chromatin interactions

Extended variants
information (count: 2010 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576504804	chr5:111838226-111838227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543995529	chr5:111838250-111838251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558839411	chr5:111838253-111838254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375158796	chr5:111838275-111838276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73223867	chr5:111838331-111838332	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541709158	chr5:111838448-111838449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548396792	chr5:111838542-111838543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563618026	chr5:111838633-111838634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145892286	chr5:111838651-111838652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188590174	chr5:111838656-111838657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563386377	chr5:111838667-111838668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530565807	chr5:111838710-111838711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552251857	chr5:111838714-111838715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs255707	chr5:111838719-111838720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs140305399	chr5:111838727-111838728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546468168	chr5:111838734-111838735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568048958	chr5:111838751-111838752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199856699	chr5:111838755-111838756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191305318	chr5:111838761-111838762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs377076295	chr5:111838850-111838851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183365704	chr5:111838866-111838867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187858033	chr5:111838867-111838868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570037956	chr5:111838891-111838892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537111524	chr5:111838892-111838893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150360329	chr5:111838893-111838894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191328562	chr5:111838901-111838902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs341290	chr5:111838912-111838913	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570472759	chr5:111838943-111838944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148723650	chr5:111838970-111838971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138033320	chr5:111839014-111839015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575247790	chr5:111839017-111839018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568594424	chr5:111839028-111839029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541804805	chr5:111839045-111839046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563090196	chr5:111839082-111839083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs255706	chr5:111839102-111839103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs255705	chr5:111839120-111839121	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563868287	chr5:111839121-111839122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568087199	chr5:111839135-111839136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528255477	chr5:111839159-111839160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546430979	chr5:111839164-111839165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568013426	chr5:111839170-111839171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs255704	chr5:111839171-111839172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183465693	chr5:111839190-111839191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187946591	chr5:111839232-111839233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192458525	chr5:111839237-111839238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146026047	chr5:111839240-111839241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35911760	chr5:111839249-111839250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539790752	chr5:111839268-111839269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570989825	chr5:111839269-111839270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185276852	chr5:111839277-111839278	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	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
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111838200-111840000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr5:111839200-111839600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:111839200-111840000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:111839200-111840000	Enhancers	Esophagus	oesophagus
5	chr5:111839200-111840000	Enhancers	Placenta	Placenta
6	chr5:111839200-111840000	Enhancers	Lung	lung
7	chr5:111839200-111840200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:111839400-111839800	Active TSS	K562	blood
9	chr5:111839400-111840000	Enhancers	Gastric	stomach
10	chr5:111839400-111840200	Enhancers	Primary B cells from peripheral blood	blood
11	chr5:111839400-111840200	Enhancers	Stomach Mucosa	stomach
12	chr5:111839800-111840000	Flanking Active TSS	K562	blood
13	chr5:111842800-111843200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:111855200-111857000	Enhancers	Primary B cells from peripheral blood	blood
15	chr5:111855600-111856000	Enhancers	GM12878-XiMat	blood
16	chr5:111855600-111856400	Active TSS	Monocytes-CD14+_RO01746	blood
17	chr5:111855600-111859400	Enhancers	Primary B cells from cord blood	blood
18	chr5:111855800-111857600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr5:111856000-111856200	Flanking Active TSS	GM12878-XiMat	blood
20	chr5:111856200-111856400	Enhancers	GM12878-XiMat	blood
21	chr5:111856400-111856600	Flanking Active TSS	GM12878-XiMat	blood
22	chr5:111856400-111856800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr5:111856600-111856800	Active TSS	GM12878-XiMat	blood
24	chr5:111856800-111857200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr5:111856800-111857400	Flanking Active TSS	GM12878-XiMat	blood
26	chr5:111857000-111857800	Flanking Active TSS	Primary B cells from peripheral blood	blood
27	chr5:111857200-111858400	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr5:111857200-111858400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr5:111857400-111857600	Enhancers	GM12878-XiMat	blood
30	chr5:111857600-111858000	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr5:111857600-111858200	Flanking Active TSS	GM12878-XiMat	blood
32	chr5:111857800-111859200	Enhancers	Primary B cells from peripheral blood	blood
33	chr5:111858000-111860600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr5:111858200-111858400	Enhancers	GM12878-XiMat	blood
35	chr5:111858400-111858600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr5:111858400-111859400	Flanking Active TSS	GM12878-XiMat	blood
37	chr5:111858400-111860600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr5:111858600-111859200	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr5:111858600-111859400	Enhancers	Stomach Mucosa	stomach
40	chr5:111858600-111859600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:111858600-111859800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr5:111858600-111859800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:111858600-111860200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr5:111858600-111860600	Enhancers	Adipose Nuclei	Adipose
45	chr5:111858800-111859200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr5:111859000-111859400	Enhancers	Esophagus	oesophagus
47	chr5:111859000-111859400	Enhancers	Small Intestine	intestine
48	chr5:111859000-111860200	Enhancers	Duodenum Mucosa	Duodenum
49	chr5:111859200-111859400	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr5:111859200-111860200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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