Tag | Content |
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EnhancerAtlas ID | HS101-47058 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chrX:48345060-48347190 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chrX:48346918-48346933 | GGGTCTGTGTGACCC | - | 6.05 | Klf1 | MA0493.1 | chrX:48346078-48346089 | AGCCACACCCA | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI048485 | chrX | 48343798 | 48349762 |
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Enhancer Sequence | CTGGTCTCGA ACTCCTGACC TCAGGTGATC CACCCACCTC GGCCTCCCAA AGTGCTGGGA 60 TTACATGCGT GAACCACCGC ACCCAGACTT CAGAACAAAT TTTTTAGGTT AAAAACCTGT 120 CTTAAAGAAA CGTCAGGGCC AGGCGTGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA 180 GGCTGAGGCA AGCGGATCAC TTGAGGTCAG GAGTTTGAGA CCAGTCTGGC CAACATAGTG 240 AAACCCGTCT CTACCAAAAA TACAAAAATT AGCTGGGTGC GGTGGCACAT GCCTGTAATC 300 CCAGCTACTC AGGAGACTGA GGCAGGAGAA TCACCTGAAC CCGGGAGATG AAGGTTACAG 360 TGAGCCGAGG TCGCGCCACT GCACTCCAGC CTGGACGACA GAGTGAGACT CTGTCTCAAA 420 AAAAAAAAGC AATGTCAGAA AGTCTACCTG GACTGCAGTC CTAAATTTCT ATAACTTAAT 480 GAACAGGAGC TGACAGAAAC TCCCCAGCTA CACGAACAGA ACTGTTTTCT ACAGCTTAAT 540 CCTGTGTCCT TAGAAATTCA CGTACTCTGT GATCCAAGGA CTATCCACGC CACAGTCCAG 600 TGACCTCAGG AGTATCCACA TACCAGTCTG CGACCCCAGC TGTTTCCACA CCTGACTGTG 660 ACTCACCCCA GTTACCATGT GTGACCCCAG GAGTATGCAC ACTCAAGTCT GGGAAAACCA 720 TTGTCCAATC TCCAGTCAGA AATGGTGTTT AAATTCTGGA GCGTGTGTTC ATAGGCATGT 780 CTACACTCCG GTCTCTGACC ACGAAAATAA CCACACCCCA GTCTGTGTGA CTCCAGGAAT 840 GTCCAGACCC CAGTTTGTGT CAGTCTAGGA GTGTCCACAC CATGGTGACT TAACCCAGGA 900 GTCTTCTCAC CGAAGTCAGT GTGACCACAG GAATGCCCAC ACCCCAATCT GTGAATATGC 960 ACAGCCCAAG AATGTATGGC GGAAGTGTCC ACACAAAAGG CCGTGTGACC ACAGGCGTAG 1020 CCACACCCAT TACAGTGCAA ATTCAGCAGC GTTCACACGA CAGCCTGTGA GACCTCAGGA 1080 GTGTCCTCAC GCCAGGTTCT GTGAGTCCAG CAGTGGCAAT GGCTTGGAGT TTCCATAGCC 1140 ATCTTAGTGG TGCCATAAAT GTGTAGCTCA AACGGTGACC ACAGAGGAGT CCACAGCTCA 1200 GTCTGTGGTG TCCTGGGAGT GGTTTTGCCC CAGTCCAGCC ACCTCAGGAG TGTCCCCACC 1260 CAAGTTTTTA TGACACAAGT AATGTCCAGT TCCCAGCATA TGTGACCCTG GTGTTGTCCA 1320 AACCCCATAG TCTCTGGCTA TTAGTGTGTC TATACCCATC TTGACGGCCT CAGGCAGGTG 1380 CACTCCCCCA TCTGTACGAC CAGAAGACTA TCGACTCCCC TGTCATTGTG ACCACAGGAG 1440 TGTAAAACTC CAGTGCCAGT GACTACTGGT GGGTCCACAT TCCAGTCTGG GTGACCCAGG 1500 GGAGGGCACA GCCCTGTCTG TGTGACCATA GGAGTCTTCA CACCCCAGTG TCTGTAAACA 1560 CACAGGAGTC AATTCCCCAG TCAGTGTGAC CAGAGGAATG TTCACACCAA ATTGTGTGAC 1620 CACAGGAGTG TCCACACCTA TCTGCATGTC CTGAGAGGTG TCTATACTCC AGTGGGTATG 1680 ACACCAACAG TGTCCACAAC AAAGTCTGTG TGACTCCAGG AGTGTCCCTC CCCCCAGTCA 1740 GTGGGAGTCT AGAAGGATCT ACACCAAGTC TTGGGAGCCC AAGGGTGTCC CTTCGCCAAT 1800 CTTTGTCACT CAGGGGACAT TCACCCCCCA GTCACACAGA CGAAGCATAT CCACAGCTGG 1860 GTCTGTGTGA CCCCAGCAGA GTCTACTTCA CAAGTCGTGT AACCACAGGA GTGTCCCCAG 1920 ACGAACCTAT GGGAATCCAG GAGTGTCCAC ATCACAGTCA CTTGACCACA GTGGTGCTGA 1980 CTTCCCAGTT TATGTATCCT TAGCCATGTC CTTTTTCCAG ACTGTGTGAC CCTAAGTGTC 2040 CACACCCCAA ACTCGGTGAT CCAAGTCACT CCAGTCTGCG TGACTCCAGT GTTGCCCACA 2100 CACCAATCTG TATGACCCTA AGAGAACACA 2130
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