Variant report

Variant	esv3374181
Chromosome Location	chr4:2799604-2802102
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	ATF2	chr4:2800024-2800854	GM12878	blood:	n/a	n/a
2	BCL3	chr4:2800167-2800462	GM12878	blood:	n/a	n/a
3	BCLAF1	chr4:2800024-2800547	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:2800557-2800835	K562	blood:	n/a	chr4:2800673-2800689
5	BHLHE40	chr4:2800129-2800807	GM12878	blood:	n/a	chr4:2800673-2800689
6	BRCA1	chr4:2800482-2800798	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:2800491-2800804	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:2799929-2800570	GM12878	blood:	n/a	n/a
9	CHD1	chr4:2800524-2800937	GM12878	blood:	n/a	chr4:2800681-2800691
10	CHD1	chr4:2801992-2802093	GM12878	blood:	n/a	n/a
11	CHD2	chr4:2800344-2800839	Hela-S3	cervix:	n/a	chr4:2800681-2800691
12	CHD2	chr4:2800220-2800976	GM12878	blood:	n/a	chr4:2800681-2800691
13	CTCF	chr4:2802032-2802151	MCF-7	breast:	n/a	n/a
14	CTCF	chr4:2801922-2802561	GM12878	blood:	n/a	chr4:2801940-2801949 chr4:2802167-2802180
15	CTCF	chr4:2801991-2802159	Gliobla	brain:	n/a	n/a
16	CTCF	chr4:2802000-2802150	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr4:2802034-2802148	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:2802080-2802230	BE2_C	brain:	n/a	chr4:2802167-2802180
19	CTCF	chr4:2801930-2802177	GM19239	blood:	n/a	chr4:2801940-2801949
20	CTCF	chr4:2801997-2802132	GM12891	blood:	n/a	n/a
21	CTCF	chr4:2801920-2802070	SAEC	small airway:	n/a	chr4:2801940-2801949
22	CTCF	chr4:2802057-2802060	GM13977	blood:	n/a	n/a
23	CTCF	chr4:2801999-2802169	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:2801987-2802172	GM19238	blood:	n/a	n/a
25	CTCF	chr4:2800587-2800666	GM19239	blood:	n/a	n/a
26	CTCF	chr4:2801980-2802130	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr4:2801920-2802070	HepG2	liver:	n/a	chr4:2801940-2801949
28	CTCF	chr4:2799766-2799829	GM19239	blood:	n/a	n/a
29	CTCF	chr4:2799700-2799850	NB4	blood:	n/a	n/a
30	CTCF	chr4:2801000-2801150	GM12872	blood:	n/a	n/a
31	CTCF	chr4:2802080-2802230	AG09319	gingival:	n/a	chr4:2802167-2802180
32	CTCF	chr4:2801951-2802190	GM12892	blood:	n/a	chr4:2802167-2802180
33	CTCF	chr4:2800720-2800870	GM12875	blood:	n/a	n/a
34	CTCF	chr4:2801987-2802183	NHEK	skin:	n/a	chr4:2802167-2802180
35	CTCF	chr4:2802054-2802136	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:2801960-2802110	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr4:2802020-2802170	HMEC	breast:	n/a	n/a
38	CTCF	chr4:2802020-2802170	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr4:2802040-2802190	NHEK	skin:	n/a	chr4:2802167-2802180
40	CTCF	chr4:2801920-2802070	GM12865	blood:	n/a	chr4:2801940-2801949
41	CTCF	chr4:2802060-2802210	AG04449	skin:	n/a	chr4:2802167-2802180
42	CTCF	chr4:2801962-2802256	K562	blood:	n/a	chr4:2802167-2802180
43	CTCF	chr4:2800439-2800515	GM19239	blood:	n/a	n/a
44	CTCF	chr4:2802000-2802150	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:2802060-2802210	HCPEpiC	choroid plexus:	n/a	chr4:2802167-2802180
46	CTCF	chr4:2802000-2802150	GM12869	blood:	n/a	n/a
47	CTCF	chr4:2802060-2802210	GM12874	blood:	n/a	chr4:2802167-2802180
48	CTCF	chr4:2799740-2799890	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:2801963-2802215	K562	blood:	n/a	chr4:2802167-2802180
50	CTCF	chr4:2800740-2800890	GM12869	blood:	n/a	chr4:2800866-2800875

No.	Distal block	Cell Line	Cell type
1	chr4:2764307..2766029-chr4:2796007..2799885,3	MCF-7	breast:
2	chr4:2799331..2801814-chr4:2936733..2939693,2	K562	blood:
3	chr4:2753714..2768807-chr4:2789818..2806638,47	MCF-7	breast:
4	chr4:2795447..2803617-chr4:2934606..2939244,18	MCF-7	breast:
5	chr4:2798466..2800490-chr4:2934363..2936581,2	K562	blood:
6	chr4:2799077..2799624-chr4:2938825..2939548,2	MCF-7	breast:
7	chr4:2798106..2801583-chr4:2843513..2845994,4	MCF-7	breast:
8	chr4:2798770..2801758-chr4:2941180..2943976,2	K562	blood:
9	chr4:2793845..2803067-chr4:2816443..2823671,22	MCF-7	breast:
10	chr4:2798786..2800390-chr4:3294087..3295620,2	MCF-7	breast:
11	chr4:2754950..2759334-chr4:2798371..2803453,5	MCF-7	breast:
12	chr4:2794525..2804465-chr4:2841103..2847851,19	MCF-7	breast:
13	chr4:2794084..2803742-chr4:2816227..2824357,23	MCF-7	breast:
14	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
15	chr4:2798213..2801828-chr4:2930948..2933812,4	MCF-7	breast:
16	chr4:2801461..2803747-chr4:2835834..2839289,3	MCF-7	breast:

Variant related genes	Relation type
SH3BP2	TF binding region
ENSG00000087274	chromatin interactions
ENSG00000087269	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000087266	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183746645	chr4:2799661-2799662	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs114511881	chr4:2799663-2799664	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs568037738	chr4:2799676-2799677	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs577918323	chr4:2799746-2799747	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs533598743	chr4:2799797-2799798	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs553731428	chr4:2799803-2799804	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs570718520	chr4:2799830-2799831	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs6812686	chr4:2799906-2799907	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs539760067	chr4:2799925-2799926	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs76687156	chr4:2799928-2799929	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs13103393	chr4:2799929-2799930	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113834258	chr4:2799948-2799949	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs555623380	chr4:2799960-2799961	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs572403732	chr4:2799998-2799999	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs541021954	chr4:2800002-2800003	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs564151777	chr4:2800027-2800028	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs559226291	chr4:2800045-2800046	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs577885328	chr4:2800085-2800086	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs141620114	chr4:2800096-2800097	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs563558208	chr4:2800158-2800159	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs529427734	chr4:2800159-2800160	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs373696741	chr4:2800169-2800170	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs548271366	chr4:2800194-2800195	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs186646829	chr4:2800216-2800217	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs146222046	chr4:2800249-2800250	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs28532194	chr4:2800256-2800257	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74636898	chr4:2800294-2800295	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs562644453	chr4:2800306-2800307	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs539765939	chr4:2800343-2800344	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs139268913	chr4:2800379-2800380	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs533279202	chr4:2800410-2800411	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs112694158	chr4:2800429-2800430	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs374618307	chr4:2800437-2800438	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs535247760	chr4:2800450-2800451	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs551685348	chr4:2800461-2800462	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs528040898	chr4:2800486-2800487	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs9994090	chr4:2800515-2800516	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs172998	chr4:2800529-2800530	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557755192	chr4:2800534-2800535	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs577583369	chr4:2800558-2800559	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs34496276	chr4:2800561-2800562	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs182658579	chr4:2800592-2800593	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs563594941	chr4:2800600-2800601	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs11722784	chr4:2800654-2800655	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542893909	chr4:2800655-2800656	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs149933456	chr4:2800685-2800686	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs567362630	chr4:2800726-2800727	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs527422582	chr4:2800727-2800728	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs28528978	chr4:2800749-2800750	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs537493990	chr4:2800772-2800773	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2795400-2801400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:2795800-2803000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:2796000-2799800	Enhancers	Primary T cells fromperipheralblood	blood
4	chr4:2796000-2802400	Enhancers	Brain Germinal Matrix	brain
5	chr4:2796000-2803400	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr4:2796000-2803600	Enhancers	Fetal Brain Male	brain
7	chr4:2796000-2803800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr4:2796200-2799800	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr4:2796200-2799800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:2796200-2800000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr4:2796200-2802000	Enhancers	Fetal Muscle Trunk	muscle
12	chr4:2796200-2802400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:2796200-2803400	Enhancers	Pancreas	Pancrea
14	chr4:2796200-2803400	Enhancers	Right Atrium	heart
15	chr4:2796200-2803600	Enhancers	Fetal Brain Female	brain
16	chr4:2796200-2813800	Enhancers	Left Ventricle	heart
17	chr4:2796400-2800600	Enhancers	Gastric	stomach
18	chr4:2796600-2803600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:2796600-2814600	Enhancers	Stomach Mucosa	stomach
20	chr4:2796800-2800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:2796800-2800000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:2796800-2800000	Enhancers	Brain Hippocampus Middle	brain
23	chr4:2796800-2800000	Genic enhancers	Fetal Stomach	stomach
24	chr4:2796800-2800400	Enhancers	Brain Anterior Caudate	brain
25	chr4:2796800-2801200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:2796800-2802200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr4:2796800-2803600	Enhancers	NHDF-Ad	bronchial
28	chr4:2796800-2803800	Enhancers	HUVEC	blood vessel
29	chr4:2797000-2800000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:2797000-2800000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr4:2797000-2800400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr4:2797000-2800400	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr4:2797000-2800400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr4:2797000-2801200	Enhancers	Fetal Thymus	thymus
35	chr4:2797000-2802000	Weak transcription	Ovary	ovary
36	chr4:2797000-2803800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr4:2797200-2800000	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr4:2797200-2800800	Weak transcription	Psoas Muscle	Psoas
39	chr4:2797200-2801200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:2797400-2801600	Enhancers	Fetal Intestine Large	intestine
41	chr4:2797400-2802200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:2797400-2802400	Enhancers	Brain Cingulate Gyrus	brain
43	chr4:2797800-2800400	Enhancers	Liver	Liver
44	chr4:2797800-2802400	Enhancers	Brain Substantia Nigra	brain
45	chr4:2798000-2800000	Weak transcription	K562	blood
46	chr4:2798000-2800600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr4:2798000-2800800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr4:2798000-2801200	Enhancers	HSMM	muscle
49	chr4:2798000-2803800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:2798200-2800400	Enhancers	Rectal Smooth Muscle	rectum

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