| Tag | Content |
|---|
EnhancerAtlas ID | HS034-24922 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr5:133846290-133848570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:133846897-133846915 | CCTTCCTGGCTTCCTCCG | - | 6.15 | | POU4F2 | MA0683.1 | chr5:133846588-133846604 | ATGCATAAATAATGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00886 | chr5:133846699-133848698 | Adrenal_Gland | | SE_06180 | chr5:133846840-133848594 | Brain_Hippocampus_Middle | | SE_18783 | chr5:133845942-133847750 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_23610 | chr5:133846319-133848715 | Colon_Crypt_1 | | SE_24106 | chr5:133846675-133848587 | Colon_Crypt_2 | | SE_27492 | chr5:133846655-133848468 | Esophagus | | SE_28095 | chr5:133846136-133848767 | Fetal_Intestine | | SE_29069 | chr5:133846123-133848878 | Fetal_Intestine_Large | | SE_31692 | chr5:133846671-133848610 | Gastric | | SE_32759 | chr5:133846492-133848541 | H1 | | SE_34361 | chr5:133844075-133849005 | HCT-116 | | SE_35006 | chr5:133846193-133848783 | HeLa | | SE_35715 | chr5:133846424-133848631 | HepG2 | | SE_40774 | chr5:133846897-133848529 | Left_Ventricle | | SE_42303 | chr5:133846695-133848663 | Lung | | SE_47397 | chr5:133836971-133849017 | Panc1 | | SE_47625 | chr5:133846758-133848644 | Pancreas | | SE_48716 | chr5:133846799-133848661 | Right_Atrium | | SE_50526 | chr5:133846651-133848689 | Sigmoid_Colon | | SE_52569 | chr5:133846320-133848665 | Small_Intestine | | SE_53502 | chr5:133847238-133848376 | Spleen | | SE_56789 | chr5:133846698-133848133 | VACO_400 | | SE_57763 | chr5:133846313-133848601 | VACO_503 | | SE_57976 | chr5:133846694-133848640 | VACO_9m | | SE_62577 | chr5:133838672-133892328 | Tonsil | | SE_65308 | chr5:133846505-133849018 | Pancreatic_islets | | SE_68727 | chr5:133846491-133848773 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I134508 | chr5 | 133844208 | 133848821 |
|
Enhancer Sequence | AGCCTCAATC TCCCAGGCTT AAGCAATCCT CCCACCTCAG CCTCCAGAGT ATCTAGGACT 60
ACAAGCAAGT GCCACCATGC CCAGCTAATT TTTGTATTTT TTAAGAGACA AGGTCTCACT 120
ATGTTGCCCA CGCTGGTCTC AAACACCTAG ACTCAAGCAA TCCTCCTCCC TTAGCCTCCC 180
GAAGTGTTAG GATTATAGGC ATGAGCCACT GGCCCTGTCC AGGGACCATT TTTATATAAA 240
CTTTCCAGTG AAATCCAGGC TGCTCTAGTC TGCCTTTTGC CTACTAGCCT CCTTGTATAT 300
GCATAAATAA TGCAGACTCA TTTTAACTTG ATGTTGATCT TACATAAAGT GTGGGTGGAA 360
AAGTATATCT GCTGGGCAAG CATCTAGTGC ATCAAATAAC GAATCCTAAA GTTAAATGGA 420
AATTATTTTT AGGTTGTCTG GGCAAATAGC ACAGAAGGTG GGGGGAATCC AGAGATATGA 480
CCTCAGATGT GACACATGCA GACACACGAC ACACCACACA TACACACACA CACACACACA 540
CACACACACG CATATGGGTA CACACAAATG CACCTTCTCT CTTCCTTCTG CCCCCACACT 600
AGCAGCTCCT TCCTGGCTTC CTCCGCCCCT CACTCACACA AAGGGCCAAA GCAAATACTT 660
CAGCACTGAG TCATGTCCTA CCTCATCTTG TTTCCAGCCT AGGAATCTCA CCTCCCCACC 720
TGGGCTGTGA GGTCTTCTGG GGCAAAGATG GTGTCTGCTT CTCCTTAGGT GTGCCCTCCT 780
AGTCTGATCA GCCAGAGGAC TGGACACCTA GGAGCTGCTT GCCTTTCCTT GAGCTCCGAG 840
GGCAGTTGAG GATCAGGGAG GCAAGGGAGC TAGATGTCCA GTGGTAGACG CTCTCTAGGG 900
CAGCCTCTTT GCCCCCCCAG GAATCTGCCT CTCCTGCCCA ACCCGGATGC CAGATAACAT 960
AGGTTTCTTT TTTCTGTAGC ACTCTCCTAG AGGAGCTGTG TTAGGTAGAT AATCTGCCTA 1020
GAGCTGGCCT AGCTGGGGAT CAACTCAACA AGAATTTCTT GTTTCCAAGC GTCTCCTTCA 1080
CATGGGCATC CAGTGCCAAT TTGTGTCCAA GTCTCTTCCC TAGCACACGG GATGGAGGTC 1140
CAGCATATTT GGAGACAGCT CACTGTGTGC CAGAGCCACA GGTCCTAGAA TATCCAGCAA 1200
TCACAGTACC CAGGGCCACC CCAGCCTCAC AAGTCACTGT GCCCAAGGCC CTGAGGGAAG 1260
AACAGCTTGC TCACTAGTGC CTGAAGGAGG CTCCCAAGGC AGCCACCTTG TACACTGGAG 1320
ACACTCCCAG CAGTGGGAGG CAGATCAAGG CCAGGACACC GTTAATGAAG CTTTGACTAG 1380
GGTGAGGCAT CTCAGGGCCA GCTGGCCTTG CTGCTTCTCA CCCCACTCTA AGCCTTGATC 1440
TGTCCACATA CTTGACCCTG TTAGAATCTG GTGTCTGCCC CTCCCCCATC CTGATGTAAC 1500
ACATCTCTGT AGCCTGAAGC CGGCCCAGTT CTTGGCTCAG AGCTACTGCG TCTGCAGCAC 1560
AGATCTGTCC CTGAGCACAG CTCGCACCAG CTTCCCTGCA GGCCTAGAGC CCAAGCCCTG 1620
GCCTCAGGCA ATCTCCGCTT CCCTTGAGGC CAGCCCAGAG CCCCAACTCA GTGAGTTCTC 1680
ATGAACTGTT TAGACTCCAC CAGGTAATGA ATTGTCCCCA CTCTGCTGTC TCAGGAGCCA 1740
GGCTGGGCCA GGTATTCTCA GATTGAATTT GTTGGGAAGA AAGGGCACTC CACCTGCTGG 1800
AGGAGGGAGC ACCTCCTGGA GGCCATGCCG CTCAGAAACT TTCTTCCCAC ACAGCTTCCA 1860
GCCCCAGGCT GCCCACCCAA GTCTCAGCAG GCCAAAGGCC TAGTGAGGCT TTTCTGTGCC 1920
CCTGCTGGAG CCCAACGTCC ATGAGAAGGC TCTAGAATGC ATTTAGGATC TGAGACTGGT 1980
CCAGCTGAAA CAGCCCAGAG AGACCCTAAT CCTGGGGCCC AGAGAGAGCC AAACAGGCCC 2040
CAGGCCACAC AGAGGGCAGC CCTGAGGCTA GCCTAGAGGG CAGGTTTCTT GCCCCTTCCT 2100
ACCAGGAGAA GCGTGTCCTT GCCACACCAA TGATGTTTCT GTCCCTGGGT GGATTCCAAG 2160
CACCTGCGGG GCAACCAGCA CTGCCCAAAT GCAGAGGGCT TCTTGGGTTC CCCCAGTAAC 2220
CCCAAGGTCG ACTCCTCCCC TCCATCTCCA CAGCTCCTGC CCCTGCCCTT CCCCCCTTCC 2280
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