Tag | Content |
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EnhancerAtlas ID | HS176-14602 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr15:99994770-99995930 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr15:99995601-99995612 | GGGCAGGTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr15:99994970-99994991 | TCTCCTTTCTGCCCCTCCTCA | - | 6.4 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_01895 | chr15:99991161-99996683 | Aorta | SE_40746 | chr15:99987956-99996889 | Left_Ventricle | SE_42455 | chr15:99989935-99996687 | Lung | SE_48915 | chr15:99990575-99996697 | Right_Atrium |
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| 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 |
GH15I099450 | chr15 | 99990613 | 99996404 |
|
Enhancer Sequence | ACCTTCCATC CAGGGCCCCG GGGATGGCAG GGCAGAGTGT GCGCTGCACA AATCCGGAAG 60 CCACCATTCA CCTCCCCTGC ACTGTGGCCC TCCCTGGCAT TGCCAAGCCT AACACATTTC 120 CCACTGAAAG CACAGCATGT GGCTGTGGAA AGTTTCCTGT GGCACCTCAG AAATTCTGCA 180 CCCACATTTG CTTTCATTTG TCTCCTTTCT GCCCCTCCTC ATTTCTGTTG GAGCTCCATC 240 CCCCTGGAGG GTTTAGGATG GGATGGATCT GGCTGGCTTG GTACGGGGGC CTCTGCCCTA 300 CCCAGGACCC ACCAGAAGCG AGCCTCCATC CTGGAACCAG GCGCTCGGCC TGGCTGACCC 360 AGCTAATCCG GGCATGGGCA GCTCAGCCAG GTCAGGAGCA TATGGCCTCC CTCCTTTGCC 420 ACTTCGTGCT GCTGATTAGG CCTCCTCCAC AAGGAGATAA ACCTGCTGGA GGAATTTGTT 480 TTCTCTGGCA GCCCACACTC TGTCCAACAG AACTGCAGGC TGACTCACTG GCGCTGGTTT 540 CCTCTGAGCC CCCGCCCATG CACGGCCTGT CCGGGCTTCT CCCTTTCAGG AGGCACTTCC 600 TGGCTTGACC TACGTGTCCT GGGAGTTTCT GTCTTGTGAT TCGGGCCCAG CTGCCACCAC 660 ATTCCTTCCG TGACACTTGG CTGGAGTGGG TGGGCAGCCG TGAGCGGGCT GGGGAATCTT 720 ATCAGAAGGT GTTCCGTCTG GGGCCTGAGC ACAGAGAGAA CTCGCCAGCC CAGGAGCTCG 780 GCTGGCAGGA GTGGAGGGCC CCCAGGGGAG GCCCCTCTCC GCAGGGAGAG AGGGCAGGTG 840 GGCAGGGCCC GTGGGGGAGA ACACACCCAA CCCACCAGTG GGGAGTGAGG CCTTGCCAGG 900 TATGAAACCG TTGGGGAAAG AATGTCCAAA CCAGCTGGTG CCTCCCTCAT TTCTATCTCC 960 AGACCAGCCC TCTCCCCTGA AATCTGGGGT CATAAATCCA ACTGCCTCCC TGACAAGCCT 1020 GCACTCCTGA TTTCTACCCC CAAAAGCTAT GTACGCCTCC CAACATCTCA GCAACTCCAT 1080 CGTTTCTTAG CTCAAGCCAA AAATCATGAT GCTATCCTTG ACTCCAAGCC TTCGGCACAT 1140 TCTACTTGCC TTTTTTTTTT 1160
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