Tag | Content |
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EnhancerAtlas ID | HS197-14493 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr3:48645140-48646590 |
Target genes | Number: 31 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr3:48646491-48646502 | AAACCACAAAC | - | 6.02 | SRF | MA0083.3 | chr3:48646317-48646333 | TTCCCTTATATGGGCT | + | 6.46 | SRF | MA0083.3 | chr3:48646317-48646333 | TTCCCTTATATGGGCT | - | 7.1 | ZNF263 | MA0528.1 | chr3:48645572-48645593 | TCATCCACCCCTTCATCCTTC | - | 6.46 |
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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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Enhancer Sequence | GCCACTGTGC CCCGCCCACA AGTGTGATGT CATTACAGGC ACAGAATGCA CAAGTAGTCA 60 AATCAGGGAT TCTGAATTAT CCATCACCAG AATAACAAAC CTTGTACCCA TTAAGTAATT 120 TCTTTTTTTT TTTTTGAGAT GGACTCTCGC TCTCTCACCC AGGCTGGAGT GCAGTGGCTC 180 CATCTCGGCT CACTGCAATC TCTGCCTCCC GGGTTCAAGC GATTCTCTTG CCTCAGTCTC 240 CCCAGGAGCT GGGATTACAG GCGTGTGCCA TGCATGGCTA ATTTTTGTAT TTTTAGTAGA 300 GATGGGGCTT CACTATGTTT GCCAGGCTGG TCTTGAACTC CTGGCCTCAG CTGATCCGCC 360 TGCCTTGGTC TCCCAAAGTG CTGAGATTAC AGGTGTGAGC CTCCAGGCCT GGACCCATTA 420 AGTAGTTTCT CATCATCCAC CCCTTCATCC TTCCAAGTCT TCACTGTCCA TCATTCCACT 480 CTCTACATCT GTATGTACGT ATTTTTTAGC TCCCACTGAT AAGTGAGAAC ATGTGATATT 540 TGCTTTCCTA AGAGATGTCA ATGCATATAC CATATATCAC ACAATCTTAG ATGAACATGT 600 ATTTCACATC TAACATCTTG GAATGCAAGA GGCATTTTAC AATCTATAGT ATCCTTTGAT 660 TAAAATTGGC AAGATTCTTG AGATTCTTTC TCTGGCACTG GAGCACAGAC AGCTCCTTAC 720 AATCTAGCAC ATTTTAGAGT TCATGTAATA TAGCATTCTT TACTATAACA AGTGACATAT 780 AACAAGGAAG TTGCAGGCCA CCTTTTCCTA TGCTTAGTAA CAATTTAAAT CGCAGGACAT 840 TGTTTCTGGA AAACTAAAAG GATGTGTCAA TAAAAACATC TGGCCCTGGG GCTGGGGGCT 900 GAAAGGAGGA GGAGATAATT ATTTCTTGGG AATCTTCTCA CCTATTCATA TATCTATCTG 960 TGACTCAAGA TTTCTTGTGT CAATTTAGAG AATTTGTATT TTTTGGAAAA TCACACATTT 1020 CATTGTACTG TTAAAATGCA TTTGCTTCCT AAAATGTATT TCTGGTCTAG CCTGGAGATT 1080 ATGACCTTGG GCAGTGAGGC TGACAGACCT GGACCCCTGC AAGTCACCTA AGGTGTCTGA 1140 ATCCCATTTT CCGCATTATA AGAGGAGACA TGATCACTTC CCTTATATGG GCTCCTTAAC 1200 AAAAGGCTGG AAAAGAATTT GGCCGCCTAC TTAACGGGCA TTATATGCTA AATAATGTTG 1260 GCTTATAGTG AAGATTGTCC CGTGAAGCCA AGGCGTGGCT AGGGTAGGGA ATGGGGCCAT 1320 TCTCGGGGTG AGTGGTCCTG GGTCCGAACC CAAACCACAA ACGGGAAGAC TCGAGCCCAA 1380 GGTCACACCC CAACCAGGGA AAAGACGGCA GGCCCAACCT GGAGGCCCTC TCCCCAAAAG 1440 CGTCCCCAAC 1450
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