Tag | Content |
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EnhancerAtlas ID | HS180-00935 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:26297530-26298780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:26298000-26298011 | AAACCACAGAG | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25494 | chr1:26294595-26302988 | DND41 | SE_30996 | chr1:26294679-26301580 | Fetal_Thymus | SE_61886 | chr1:26280771-26325644 | Toledo | SE_66821 | chr1:26297269-26298717 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 26297775 | 26298514 | chr1 | 26297632 | 26298516 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025970 | chr1 | 26297127 | 26298958 |
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Enhancer Sequence | GTGACTTCAA ATATCTAGGG AACTGCCAGG TGCCGTCTGA GGCTTCTATG GGTAGCTCTT 60 GAGGGGTTAA CCTGGGCAAG TAGAGGAGGG TTACAAACTA GGAGATCTTG CTCTTAGGTT 120 AGAGTTAAGT CAAACCTTTG AAATTCAGAC AAGCCTGGCT CCTTTCTCAT GGAAACTGCC 180 CTGCACACAG CACCTGCTGA GGGATCAGAA AGGGACCTCT GATGCAGAGA GCTCAGAGCC 240 TAGCTGGGAC GGGGCTACAG TGTGTTCTGG TGGGCAAAGA GGAGCTGATA CAATCAAATT 300 GCCTCTCTTG GAAATCTGTT CAAAGAAATC CAAAAAAATA TGGCAGTGAG CAGTGGGAGC 360 TGAAGATGAA AGGATGCCGC AAGCTAAAGG GAACACACTC TGAGTGGTTC AAGCCGAGTG 420 AAGTTATGAG GAAGCAGAAA TGGAATAAAC AGCTGCTATC AGTGAGAGAA AAACCACAGA 480 GCAGAAAAAA AAATGCATAA CGGAACAAAG AAAAAGAGAT GTCGTGAGAG GAAGACACAG 540 AGAGACTGAA CCCATGAGAC AGACGGAAAG AAAAGTCAGT CCTGCCAGCC ACCCTGATTT 600 CTATAACTGC ACTCCCACCC AGTCCAGGTG CACTCTCATA AACAAACTCC CCTTTTTTTC 660 TCAAGCTAAG TTTGTGAACC TCTAGTCTTT GTAACCAATA AAGCTTAATA AGAGGATGCC 720 TCCTCTGGGT GGAAGCTGGA CCATGGACCT CTGCAGGCCT CGCCCTTTAG CTGCTCTATG 780 ACTGATGACA TTATTCATAG TCCTTCCATG CTTTGTTTCT TTAAAACACT TCCATAAATT 840 TAGCCCGTTA TCCTCATAAA CTCCCCTACA ATGCAGATAA GGTGGGCAAT AATGAGTCTG 900 GGTAAGGAGA GAGGTGGTGG AGTAGAGAGA GGTGAATACT CCATTTACAG GGAGGAAACC 960 AAGGTTCAGA GAGGTTAAAT GACTAGGCCA GGTCATTCTG CAAGTAAGAT AGTCAGGATC 1020 TCCAAACTTT CAGTTAAGTA TTTTTTCTTA TTTATTTGTT TAATTATTTA TTTAGAAACA 1080 AGGTCTTGCT CTGTTGCTCA GACTGGAGTT CAGTGGTGCA ATCATGGCTC ACTGCAGCCT 1140 AGACCTCCTA GGCTTAACTG ATCCTCCCAC CGTAGCCTCT CGAGTAGCTG GGACTATAGG 1200 TGTGTGCCAC CACACCCAGC TAATTTTTTT TTTTTTTTGG TAAAGATAGA 1250
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