Tag | Content |
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EnhancerAtlas ID | HS091-24554 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:50009130-50010530 |
Target genes | Number: 40 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:50010002-50010021 | AGGTCAGTAGGGGGCACTA | + | 6.23 | Foxd3 | MA0041.1 | chr19:50009253-50009265 | GTTTGTTTGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr19:50010300-50010321 | CTTCCCCTTCCCCTCTCCTCT | - | 6.04 | ZNF263 | MA0528.1 | chr19:50010283-50010304 | TTCTCCTTCCCCTCCCCCTTC | - | 6.09 | ZNF263 | MA0528.1 | chr19:50010293-50010314 | CCTCCCCCTTCCCCTTCCCCT | - | 6.19 | ZNF263 | MA0528.1 | chr19:50010275-50010296 | CCTTCCCCTTCTCCTTCCCCT | - | 6.2 | ZNF263 | MA0528.1 | chr19:50010287-50010308 | CCTTCCCCTCCCCCTTCCCCT | - | 6.37 | ZNF263 | MA0528.1 | chr19:50010274-50010295 | CCCTTCCCCTTCTCCTTCCCC | - | 6.51 | ZNF263 | MA0528.1 | chr19:50010268-50010289 | TCCTTTCCCTTCCCCTTCTCC | - | 6.62 | ZNF263 | MA0528.1 | chr19:50010286-50010307 | TCCTTCCCCTCCCCCTTCCCC | - | 6.97 | ZNF263 | MA0528.1 | chr19:50010292-50010313 | CCCTCCCCCTTCCCCTTCCCC | - | 6.98 | ZNF263 | MA0528.1 | chr19:50010271-50010292 | TTTCCCTTCCCCTTCTCCTTC | - | 7.36 | ZNF263 | MA0528.1 | chr19:50010280-50010301 | CCCTTCTCCTTCCCCTCCCCC | - | 8.01 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_68187 | chr19:49976788-50037595 | TC32 | SE_68188 | chr19:49976788-50037595 | TC32 | SE_68189 | chr19:49976788-50037595 | TC32 | SE_68190 | chr19:49976788-50037595 | TC32 | SE_68191 | chr19:49976788-50037595 | TC32 | SE_68192 | chr19:49976788-50037595 | TC32 | SE_68193 | chr19:49976788-50037595 | TC32 | SE_68194 | chr19:49976788-50037595 | TC32 | SE_68464 | chr19:49990162-50019336 | TC71 | SE_68465 | chr19:49990162-50019336 | TC71 | SE_68466 | chr19:49990162-50019336 | TC71 | SE_68467 | chr19:49990162-50019336 | TC71 | SE_68468 | chr19:49990162-50019336 | TC71 | SE_68469 | chr19:49990162-50019336 | TC71 | SE_68470 | chr19:49990162-50019336 | TC71 | SE_68471 | chr19:49990162-50019336 | TC71 | SE_68472 | chr19:49990162-50019336 | TC71 | SE_68473 | chr19:49990162-50019336 | TC71 | SE_68474 | chr19:49990162-50019336 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 50010362 | 50010419 | chr19 | 50010162 | 50010372 | chr19 | 50009848 | 50010361 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I049506 | chr19 | 50009793 | 50010480 |
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Enhancer Sequence | TTGCAGTGAG CCGAGATCGC ACCACTGCAC TCCAGCCTGG GTGACAGACA GAGACTCCGT 60 CTCAAAAAAA AAAAAAAAAA AGAAATAGGT TGGTGCAAAA GCAATTGTGG TTTTTTGTTT 120 GTTGTTTGTT TGTTTTTGAG TCTCACTCTG TTGCCCAGGC TGGAGTGCAG TGGCACAATC 180 TCATCTCACT GCAACCTCTG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC ACCCTCCCAA 240 GTAGCTGAGA TTACAGGTGC CCACTACCAT GTCTGGCTAA TTTTTGTATT TGTAATAGAG 300 ATGGGGTTTT GCCATGTTGG CCAGGCTGGT CTCAAACTCC CGACCTCAGC CTCCCAAAGT 360 GCTGGGATTA CAGGCGTGAG CCACCGTGTC TAGCCAGCAA TTGCGGGTTT TTTGTTTGTT 420 GGTTTTTTTC AGATGGAGTC TTGCTCTGTC ACCCAGACTG AAGTGCAGTG GCACAATCTC 480 GGCTCATTGT AACTTCCGCC TCCCAGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT 540 AGCTGGGACT ATTCAGCGAG TGCCACCATG CCTGGCTAAT TTTTGTATTT TTAGTAGAGA 600 CAGGGTTTCA CCATGTTGGC CAGGCTGGTC TGGAACTCCT GACCTCGTGA TCCGTCTGCC 660 TCGGCCTTCC AAAGTGCTGG GATTATAGGC GTGAGCCACC GTGCCCGGCC TGCAATTGGG 720 GTTTTAATGG CAGAAACCGC AATTACTTTT GCACCACCCT AATATAAAGA CACAATTATT 780 ATCCCCATTT TCCAGATAAA GAACCTTTGG CTGGGAGAGG TGTACCTGGA AGAGTCGTGT 840 TTTGGTTTTG AACTCAGGTG TGATTGCCCC CCAGGTCAGT AGGGGGCACT ATTGTGTAAG 900 GGTGGAGAGG AGGGGCAGCG GTTAGGTGGT TCAGGGTGCA CAGCTCAAAG CTGCCTGGGG 960 CCATTCTAGG CACAGAGGCA GGGGCCAGGG CCGGCTTTAA GGCCAGCTCC TCGTGCAGTC 1020 TGAGGAGTGG ATCAGAAGGG ACCAGCACCT GGTGAGTGCT CTACTTGAAC CATCTTGAAA 1080 CTGGAACCAA GGGGACCACA TTTTTGTTTT ATGCTGAGTG TGTCCTGCCA TGGGCTTTTC 1140 CTTTCCCTTC CCCTTCTCCT TCCCCTCCCC CTTCCCCTTC CCCTCTCCTC TTCTCTTCTC 1200 TTCCGTTTTT TGGAGACGGA GTCTTGCTCT GTCGCCCAGG CTGGAGTTCA ATAGCGCAAT 1260 CTCGGCTTAC TGCAACCTCC GCCTCCTGGG TTCGAGTGAT TCTCCTGCCT CAGCCTCCCG 1320 AGTAGCTGGG ATTACAGGTG CGCACTACCA CGTCCGGCTA ATTTTTGTAT TTCTAGTAGA 1380 GACGGGGTTT CACCACGTTG 1400
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