| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22147 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr18:29628200-29630450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr18:29628369-29628387 | CAAAAGCGAAACTCTATC | + | 6.4 | | IRF9 | MA0653.1 | chr18:29628367-29628382 | AACAAAAGCGAAACT | + | 6.52 | | ZNF263 | MA0528.1 | chr18:29629565-29629586 | CGGGGAGGAGGAGGATGGGGA | + | 6.49 | | ZNF263 | MA0528.1 | chr18:29629571-29629592 | GGAGGAGGATGGGGAAGTGAA | + | 7.36 | | ZNF263 | MA0528.1 | chr18:29629568-29629589 | GGAGGAGGAGGATGGGGAAGT | + | 7.69 |
|
| | 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 |
| GH18I032047 | chr18 | 29627919 | 29631200 |
|
Enhancer Sequence | CCTGTCTCTA CTAAAAATAC AAAAAAAAAA AAAAAAAAAT TAGCCGGGTG TGGTGGGGGG 60
CACCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CCTGGGAGAC 120
GGAGGTTGCA GTGAGCTGAG ATCACGCCAT TGCACTCCAG CATGGGCAAC AAAAGCGAAA 180
CTCTATCTCA AAAAACAAAC AAAAAAACCC AAAAAAACCT GTCTCAAAAA AAAAGAGAGA 240
AAATCCTCAC AGCAATCCTA TGAGATAGGC TTGATGATTA TCCCCATTTT AAAAATGATA 300
AACTGAGACT CAGAGAGGTT AAGTCAATCA TACAAGGTCA CACAGCTGGT AAGTAACAAA 360
GACAGAATTT GAATACAGTG ATCTAGCTCC AGGGCTGTGT GGGAAACCCC TGTGGTCTAT 420
AGCAAGTTCA AGAGAAAAGC ATGCAGAGAT ATTTGTTATT GATCTTAATG GCCTAGGGAG 480
TTGGCAATTG GAATGGCTAA GTAGGAGCTT GTTAGGTGTT GAGGGAGCAG AGCCGATGGT 540
CACGGGCTTT TCCTGCTCAA GTTGCTCTGT AGGAGGAACT GGGCTAGGGA GTTGTTTCAC 600
AATAGGTCCC TGGGGAGCTA GAGGAAGTTA GAAGAAAGCA TAAGGATGGA ATGATAGTGA 660
CTACTATCAC TGAGTTTACT GAGTTATAAG TATTTTCTTG TCTCCTAGCA ACTCTGTGAA 720
GAAGGTTGAA CCCTGACCAT TAGTACCCAG GGTGCTGCTT TGGCTGGAAG AATGCCAGGC 780
CCTCTGGACT GTGGTCCTAG GCTGCATCTA AGCAGCAATC TGGGGCAGGC CGTGTACTGG 840
TCAGTTCCGT GGTACTGTGT ACCTGCTCCA GCAGAAATCC AGTCCACATG CTGCTCAGTT 900
TGGCCCAAAT TGAAGGTGGC CCATGAAGCT AGGTCCTCCA TGATTTTACA GGTCTTCAGG 960
GTCATTGAAG ACAGCTGACC TAAGCAGGGA AACAAACTAG GAATGGTGGA ATCAGATTGC 1020
CTGTGGGATT TTGTAGTTAA ATCCTAGGCT TTAAAGGGGA TAGGCTTGGT TCTAATCCCA 1080
GGAAGTCTAT TAAATTCTGT CACTGTTTCA TCATTTGTAA AATGGGGATG GTGATGACAT 1140
TCATGCCTTT TTCACAAGTA GTAAATGAAT CAGGCATATA ATAAAGTAAG CACTCTGTCT 1200
CCTGGTGATC ACTCCATTAA TAGAAGAGGG TGGTGGTGAT AGTGGAGGTT CACTACACTT 1260
TTTCAATTCT ATAAAATCAG GCCTAGAGAA GATTTCTTAG AGGAAGTGAT GTCCTCTCAC 1320
AGTTAGAGAA CCCACATGGG GTGGTGGTGT GAGTCGGGGG GGTGGCGGGG AGGAGGAGGA 1380
TGGGGAAGTG AAGTGGTAAA ATCTCACCAC AAAGACCAGG ATGCTATCAT GGCCTTGAAG 1440
CAGGAGCAGA TTGTTCAGAA ATCCAAGGTT CTGTAATACC CTAGGGCTGT CTAGAGGTGG 1500
TAATTGGAAC ACAAGACCTT CAGGTGTCCT GTGTTAGTGT TTCACTCTTG AGCAGAAGCT 1560
CAGGAGCATG TCACTCTGAA GGATCTAGAG CCACTAGAAG TCATGATTTA CCCCATGGTT 1620
AGGAAAAGGC AGGGGACAGA TATGTGGTAT AGCTGGGGTT CACGTGCTTA GGGGTCCCTA 1680
ATGGGGACAT GTGGGTGAAA ACACACTGAG GGAAGTCCTG GGCAAGGAGG GCTGGGTCCA 1740
ATGCTGATTC TGGATGGGTG TGGAAGTTAA CCAGGAATTA TTGCTTTAAA GGACTGGATT 1800
ACAGGTTTTG CAAGCAGATA AGATCAGTGA CATCATCTGA CTTACCTCAC ATAAGAGGTT 1860
TCCTGGCATT TAGAGATTTC CTGGGTAAAT GATTCTTCTG ACTTCCAAAA ATAATTAGAT 1920
AACTCAGAGA TCAAACCACA AGATAACCAT CTTTTCTTTC TGAGCTGCTC AAGAATGATA 1980
AAATGTTTGT TAAAAACATC AGGGGATTTT GACTTTTCTT ATATGCATCC TTAAGAGCCA 2040
ATAGCTCCTT TTTGTCAAGC AGTAATTATA TTGTTATATT CTGCCATTTT TTAAAATTTG 2100
GAGACAGGGT CTCGCTCTGT CACCCAGGCC GGACCGCAGT GGTGCAGTAA TAGCTCACTG 2160
TAACCTTGAA CTCCTGGGCT CAAGTGATCC TTACCTCAGC TTCCTGAGTA GCTGGAACTA 2220
CAGGTGTGCA CCTTCACAAC TGGATAATTC 2250
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