Variant report

Variant	esv1794440
Chromosome Location	chr4:69369246-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:672)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
7	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
8	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
9	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
10	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
11	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
12	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
13	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
16	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
17	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
18	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
21	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
22	CEBPB	chr4:69574361-69574618	HepG2	liver:	n/a	chr4:69574511-69574522
23	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
24	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
25	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
26	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
27	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
28	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
29	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
31	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:69568931-69569294	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
34	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
36	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
37	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:69574389-69574642	A549	lung:	n/a	chr4:69574511-69574522
39	CEBPB	chr4:69580237-69580432	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
41	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
42	CHD1	chr4:69583916-69583936	GM12878	blood:	n/a	n/a
43	CTCF	chr4:69443420-69443570	SAEC	small airway:	n/a	n/a
44	CTCF	chr4:69537760-69537910	GM12873	blood:	n/a	n/a
45	CTCF	chr4:69537097-69537207	Fibrobl	skin:	n/a	n/a
46	CTCF	chr4:69537320-69537470	NHEK	skin:	n/a	n/a
47	CTCF	chr4:69434820-69434970	GM12872	blood:	n/a	n/a
48	CTCF	chr4:69537320-69537470	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:69537116-69537164	GM12878	blood:	n/a	n/a
50	CTCF	chr4:69443397-69443544	GM19240	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435593-69435643	HMEC	breast:	n/a
2	chr4:69435593-69435643	HMEC	breast:	n/a
3	chr4:69537806-69537856	HCPEpiC	choroid plexus:	n/a
4	chr4:69537826-69537876	MCF-7	breast:	n/a
5	chr4:69536319-69536369	HUVEC	blood vessel:	n/a
6	chr4:69435250-69435300	Hepatocyte	liver:	n/a
7	chr4:69537589-69537639	HRE	kidney:	n/a
8	chr4:69381368-69381418	HRCEpiC	kidney:	n/a
9	chr4:69434475-69434525	T-47D	breast:	n/a
10	chr4:69522639-69522689	HCF	heart:	n/a
11	chr4:69435250-69435300	NHBE	bronchial:	n/a
12	chr4:69537826-69537876	K562	blood:	n/a
13	chr4:69537806-69537856	SK-N-MC	brain:	n/a
14	chr4:69435593-69435643	T-47D	breast:	n/a
15	chr4:69536319-69536369	GM12892	blood:	n/a
16	chr4:69435593-69435643	Hela-S3	cervix:	n/a
17	chr4:69514031-69514081	Jurkat	blood:	n/a
18	chr4:69522639-69522689	T-47D	breast:	n/a
19	chr4:69536319-69536369	NHBE	bronchial:	n/a
20	chr4:69537826-69537876	AG09309	skin:	n/a
21	chr4:69514031-69514081	H1-hESC	embryonic stem cell:	embryo
22	chr4:69537589-69537639	HL-60	blood:	n/a
23	chr4:69514031-69514081	MCF-7	breast:	n/a
24	chr4:69522639-69522689	HL-60	blood:	n/a
25	chr4:69537589-69537639	H1-hESC	embryonic stem cell:	embryo
26	chr4:69435601-69435651	AG04449	skin:	fetal
27	chr4:69435593-69435643	HEK293	kidney:	embryo
28	chr4:69435250-69435300	SK-N-MC	brain:	n/a
29	chr4:69435250-69435300	NB4	blood:	n/a
30	chr4:69522639-69522689	SK-N-SH_RA	brain:	n/a
31	chr4:69435250-69435300	AG09309	skin:	n/a
32	chr4:69536319-69536369	Hepatocyte	liver:	n/a
33	chr4:69381368-69381418	RPTEC	kidney:	n/a
34	chr4:69434475-69434525	K562	blood:	n/a
35	chr4:69537589-69537639	AG09319	gingival:	n/a
36	chr4:69537806-69537856	HCM	heart:	n/a
37	chr4:69537806-69537856	HRPEpiC	eye:	n/a
38	chr4:69536319-69536369	HEEpiC	esophagus:	n/a
39	chr4:69536319-69536369	H1-hESC	embryonic stem cell:	embryo
40	chr4:69435593-69435643	AG10803	skin:	n/a
41	chr4:69434475-69434525	GM19239	blood:	n/a
42	chr4:69435593-69435643	HRPEpiC	eye:	n/a
43	chr4:69522639-69522689	HRE	kidney:	n/a
44	chr4:69537806-69537856	HAEpiC	amniotic membrane:	n/a
45	chr4:69435250-69435300	MCF-7	breast:	n/a
46	chr4:69435250-69435300	AG10803	skin:	n/a
47	chr4:69514031-69514081	HEK293	kidney:	embryo
48	chr4:69381368-69381418	GM12892	blood:	n/a
49	chr4:69435250-69435300	HRE	kidney:	n/a
50	chr4:69435593-69435643	NHDF-neo	bronchial:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
3	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
4	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
5	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
2	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
3	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
4	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
5	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
6	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000248635	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000248635	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island

Extended variants
information (count: 5551 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5551 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535236610	chr4:69369253-69369254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181881495	chr4:69369329-69369330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568671030	chr4:69369353-69369354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138361716	chr4:69369369-69369370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186587532	chr4:69369378-69369379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527459470	chr4:69369383-69369384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546159361	chr4:69369438-69369439	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62317919	chr4:69369442-69369443	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573280989	chr4:69369493-69369494	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542005927	chr4:69369494-69369495	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190745474	chr4:69369499-69369500	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530628008	chr4:69369502-69369503	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544067796	chr4:69369510-69369511	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180936358	chr4:69369536-69369537	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571004330	chr4:69369545-69369546	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186162336	chr4:69369569-69369570	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76313738	chr4:69369579-69369580	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4546319	chr4:69369611-69369612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143673755	chr4:69369631-69369632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147189297	chr4:69369632-69369633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549107187	chr4:69369648-69369649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191499153	chr4:69369666-69369667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182757484	chr4:69369746-69369747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557618121	chr4:69369748-69369749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550234554	chr4:69369827-69369828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187304939	chr4:69369850-69369851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140846974	chr4:69369854-69369855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573159602	chr4:69369861-69369862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542269626	chr4:69369862-69369863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4464628	chr4:69369891-69369892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575069019	chr4:69369902-69369903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190599897	chr4:69369912-69369913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183233695	chr4:69369941-69369942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533251835	chr4:69369946-69369947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540159424	chr4:69369956-69369957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528565418	chr4:69369962-69369963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565822988	chr4:69370021-69370022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56853574	chr4:69370030-69370031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528894898	chr4:69370051-69370052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549068527	chr4:69370109-69370110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376718221	chr4:69370135-69370136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189231746	chr4:69370137-69370138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192177938	chr4:69370141-69370142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551189667	chr4:69370173-69370174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571005347	chr4:69370194-69370195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540078666	chr4:69370248-69370249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184496742	chr4:69370267-69370268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566824516	chr4:69370275-69370276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187874228	chr4:69370366-69370367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28809933	chr4:69370371-69370372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69365200-69370400	Weak transcription	Liver	Liver
2	chr4:69369400-69369600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:69370200-69370600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:69370400-69370800	ZNF genes & repeats	Liver	Liver
5	chr4:69370600-69371200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:69370600-69371200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr4:69370800-69371200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr4:69370800-69371200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:69370800-69371200	Enhancers	Gastric	stomach
10	chr4:69370800-69371200	Enhancers	Spleen	Spleen
11	chr4:69370800-69372000	Weak transcription	Liver	Liver
12	chr4:69371000-69371200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr4:69371200-69372200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr4:69372200-69372400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr4:69373400-69373800	Enhancers	Fetal Heart	heart
16	chr4:69373800-69374200	Weak transcription	Fetal Heart	heart
17	chr4:69374200-69375200	Enhancers	Fetal Heart	heart
18	chr4:69388400-69389000	Enhancers	NHEK	skin
19	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
23	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
25	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
26	chr4:69403400-69404800	Strong transcription	Liver	Liver
27	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
30	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr4:69404800-69406800	Weak transcription	Liver	Liver
33	chr4:69405600-69406800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
34	chr4:69406200-69407000	Strong transcription	Duodenum Mucosa	Duodenum
35	chr4:69406800-69407800	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr4:69406800-69409200	Strong transcription	Liver	Liver
37	chr4:69407000-69413800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:69407800-69408200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
39	chr4:69408200-69408600	Enhancers	HepG2	liver
40	chr4:69408200-69409200	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr4:69409200-69413600	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr4:69409200-69418800	Weak transcription	Liver	Liver
43	chr4:69413600-69418800	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr4:69417200-69418400	Enhancers	NHEK	skin
45	chr4:69417800-69418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:69417800-69419200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:69417800-69420600	Enhancers	HepG2	liver
48	chr4:69418600-69419200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:69418800-69419200	Enhancers	Liver	Liver
50	chr4:69418800-69421800	Weak transcription	Rectal Mucosa Donor 31	rectum

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