| Tag | Content |
|---|
EnhancerAtlas ID | HS048-30122 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:133846060-133848650 |
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: 2 | Chromosome | Start | End |
| chr5 | 133846500 | 133848623 | | chr5 | 133846400 | 133848045 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I134508 | chr5 | 133844208 | 133848821 |
|
Enhancer Sequence | ACGTGCCCAT TGCTATGTCA TGTGTGGGTG AAATAAGGGG CTGACACTCC CAGTAGCCAT 60
AGAGGGTCCT TTTTCATTTT ATCATTATCC CCAACAATGC TGTGATCACC AATCCAGGCA 120
CACTGTCCAA TTTTGTCATC CACCTTGGAA TCTTTTTTTT TTTTTTTTGA GATAGGGCTC 180
TTGCTCTGTC ACACAGGCTG GAGGGCAGTG GTGTGATCAC AGCTCACTGC AGCCTCAATC 240
TCCCAGGCTT AAGCAATCCT CCCACCTCAG CCTCCAGAGT ATCTAGGACT ACAAGCAAGT 300
GCCACCATGC CCAGCTAATT TTTGTATTTT TTAAGAGACA AGGTCTCACT ATGTTGCCCA 360
CGCTGGTCTC AAACACCTAG ACTCAAGCAA TCCTCCTCCC TTAGCCTCCC GAAGTGTTAG 420
GATTATAGGC ATGAGCCACT GGCCCTGTCC AGGGACCATT TTTATATAAA CTTTCCAGTG 480
AAATCCAGGC TGCTCTAGTC TGCCTTTTGC CTACTAGCCT CCTTGTATAT GCATAAATAA 540
TGCAGACTCA TTTTAACTTG ATGTTGATCT TACATAAAGT GTGGGTGGAA AAGTATATCT 600
GCTGGGCAAG CATCTAGTGC ATCAAATAAC GAATCCTAAA GTTAAATGGA AATTATTTTT 660
AGGTTGTCTG GGCAAATAGC ACAGAAGGTG GGGGGAATCC AGAGATATGA CCTCAGATGT 720
GACACATGCA GACACACGAC ACACCACACA TACACACACA CACACACACA CACACACACG 780
CATATGGGTA CACACAAATG CACCTTCTCT CTTCCTTCTG CCCCCACACT AGCAGCTCCT 840
TCCTGGCTTC CTCCGCCCCT CACTCACACA AAGGGCCAAA GCAAATACTT CAGCACTGAG 900
TCATGTCCTA CCTCATCTTG TTTCCAGCCT AGGAATCTCA CCTCCCCACC TGGGCTGTGA 960
GGTCTTCTGG GGCAAAGATG GTGTCTGCTT CTCCTTAGGT GTGCCCTCCT AGTCTGATCA 1020
GCCAGAGGAC TGGACACCTA GGAGCTGCTT GCCTTTCCTT GAGCTCCGAG GGCAGTTGAG 1080
GATCAGGGAG GCAAGGGAGC TAGATGTCCA GTGGTAGACG CTCTCTAGGG CAGCCTCTTT 1140
GCCCCCCCAG GAATCTGCCT CTCCTGCCCA ACCCGGATGC CAGATAACAT AGGTTTCTTT 1200
TTTCTGTAGC ACTCTCCTAG AGGAGCTGTG TTAGGTAGAT AATCTGCCTA GAGCTGGCCT 1260
AGCTGGGGAT CAACTCAACA AGAATTTCTT GTTTCCAAGC GTCTCCTTCA CATGGGCATC 1320
CAGTGCCAAT TTGTGTCCAA GTCTCTTCCC TAGCACACGG GATGGAGGTC CAGCATATTT 1380
GGAGACAGCT CACTGTGTGC CAGAGCCACA GGTCCTAGAA TATCCAGCAA TCACAGTACC 1440
CAGGGCCACC CCAGCCTCAC AAGTCACTGT GCCCAAGGCC CTGAGGGAAG AACAGCTTGC 1500
TCACTAGTGC CTGAAGGAGG CTCCCAAGGC AGCCACCTTG TACACTGGAG ACACTCCCAG 1560
CAGTGGGAGG CAGATCAAGG CCAGGACACC GTTAATGAAG CTTTGACTAG GGTGAGGCAT 1620
CTCAGGGCCA GCTGGCCTTG CTGCTTCTCA CCCCACTCTA AGCCTTGATC TGTCCACATA 1680
CTTGACCCTG TTAGAATCTG GTGTCTGCCC CTCCCCCATC CTGATGTAAC ACATCTCTGT 1740
AGCCTGAAGC CGGCCCAGTT CTTGGCTCAG AGCTACTGCG TCTGCAGCAC AGATCTGTCC 1800
CTGAGCACAG CTCGCACCAG CTTCCCTGCA GGCCTAGAGC CCAAGCCCTG GCCTCAGGCA 1860
ATCTCCGCTT CCCTTGAGGC CAGCCCAGAG CCCCAACTCA GTGAGTTCTC ATGAACTGTT 1920
TAGACTCCAC CAGGTAATGA ATTGTCCCCA CTCTGCTGTC TCAGGAGCCA GGCTGGGCCA 1980
GGTATTCTCA GATTGAATTT GTTGGGAAGA AAGGGCACTC CACCTGCTGG AGGAGGGAGC 2040
ACCTCCTGGA GGCCATGCCG CTCAGAAACT TTCTTCCCAC ACAGCTTCCA GCCCCAGGCT 2100
GCCCACCCAA GTCTCAGCAG GCCAAAGGCC TAGTGAGGCT TTTCTGTGCC CCTGCTGGAG 2160
CCCAACGTCC ATGAGAAGGC TCTAGAATGC ATTTAGGATC TGAGACTGGT CCAGCTGAAA 2220
CAGCCCAGAG AGACCCTAAT CCTGGGGCCC AGAGAGAGCC AAACAGGCCC CAGGCCACAC 2280
AGAGGGCAGC CCTGAGGCTA GCCTAGAGGG CAGGTTTCTT GCCCCTTCCT ACCAGGAGAA 2340
GCGTGTCCTT GCCACACCAA TGATGTTTCT GTCCCTGGGT GGATTCCAAG CACCTGCGGG 2400
GCAACCAGCA CTGCCCAAAT GCAGAGGGCT TCTTGGGTTC CCCCAGTAAC CCCAAGGTCG 2460
ACTCCTCCCC TCCATCTCCA CAGCTCCTGC CCCTGCCCTT CCCCCCTTCC CAGTCTTGCT 2520
CCCTACATAC TCCAGTACAA GCAAATTCAT GAATTCGGTA CATACATTTC CAGACCTTTT 2580
TTTCCCGTAC 2590
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