| Tag | Content |
|---|
EnhancerAtlas ID | HS091-13455 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr14:66961820-66963540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:66962377-66962396 | AGCCCAGTAGGTGGCACCA | + | 6.34 |
| | | 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 |
| GH14I066495 | chr14 | 66962321 | 66962470 |
| Enhancer Sequence | GTTTGAAATA ATTGAAAAGG CAATAATTTT CTCACTGTGA TTTATAGTAT TTAATGCCTT 60
GTCCCAACAC CGAAATTTAT CCCAATTGCC ACCTAAAATC ATCTCATCAT CAAATTTTGG 120
CAAATTGTAA TTTAAGGAAA AAAGCACTGA ATTTAAGACT CAGATACATG AGTTGCAGGC 180
CTTCCTCTGA GGCTCACCAG TTATATGACT TGGAAAAGTC ATTTAATTTC AGGTTTTAAA 240
AATACAAACA ACATTAACAT GGAGCATGCT GAGAACTTAA TACCTTGTGC AACCCTCACA 300
GTGACTCTAT GAAAGGTATT ATAGAACAAG AAACAAGCTC AGAGAAGCCA GGCTTCTTGG 360
CTCCATATTC AATCCTTATT CCCTAGACTA TGCTACAAAA TGGATGTGTA AAAGCATGTG 420
ACTTTTCATG CCTCTTCTAG ATCTAAACGC TATAATTTGA ATCCAAATTT ATTATCTGTT 480
TAACGTATAA TCTTCTCAGT GAAGAAGCAT ACTCCTAAGG TTAATTTGTT CAGTAAGAAA 540
ATGTTAACTC TGCATTTAGC CCAGTAGGTG GCACCAACCA CATCCAGGCT TCAAGTCCAC 600
AGAGTGGTAA TTCAGGAACC ATGAAATGCT GTGGGAGAGA TCGGTCTTCT ATTACTCTCA 660
GGACAAAAGG TGCCACATTC ATGTATCAAA TGAAAAAAGA AAAAAATTTC TTGATGTTTT 720
ATCACATGCT CTTTTGGCAC CAAGGTGTAT TACTGGCAGC CTTGATTAGA CCATGTTAAA 780
CTCAGTGTTC TGTTGCATAA TTTTTACCTA GTATTTTACT CCCTGTACTA CAGTTATCTC 840
CATTTCAAAA AACAGTCACT GCCCACTTCC TCCACAATCC TTGTAGAATA GTGTTCCCTT 900
CCACCACAGA TAAATCAGGC GATTGGGGCA CTAAAAGAAA AAATGAGCAC TAAACAAAAA 960
ATAAAAGATG GTGCTTATTT GAAGTTTGTA TACTTAACAG TGTTACAGGA CAGCGTTTCT 1020
TTTTCTCTAG TTTCAAAAGA ATTGAATTGC ACAAACCTGT CTTAGAGAAA GGGTGGAATA 1080
TAATTTTGGA CACACCTCTC AGTAAATCAG GGTACAGGCT TTTCTGTTCT AAGCATTTCC 1140
AAGTAGATGA AGAGTTTACC TCAGTACTCT TAGCCAAGAA TTCCTCCTCC CACTGTCCGA 1200
TGTGCTGGTT GGCTGAGTTG CAGTGGTATG ATCTGTGTAG CTGGCAAAAT ACAATCCTGT 1260
GTTAATATTA CTGATTTTGT TACACTTCAA CAAATCCCTA CTTGTGAATT CCCTTGATGC 1320
CCAGGATGTG GCATTACCGT CATCCATGTT ATCTCTTTGG CATGCTGCCT CACTTAGTCT 1380
GTTTATACCT ACGATGAAGT CTTTACTTTT GATCTTTCCG GAGACAGGTG ACATTTGAAA 1440
GGATTTACTT TTCCACCAGT GTAAAATTAT AATTTGATTC AGGGTGTATT GTAGGCCCTC 1500
CCTAACTTCT ATAGAGTCCA GAAGGCAAGT TTGTGGACTT TGGCAGTCAC CTATCTTAGA 1560
GAGCACAGGT GCTAAGCAAT CTCTAAATTC AACTGAATTT CCCATCATAT CTGCTGGTGT 1620
TTAAAGAAGA GGTTTATCTT CAGCAATAAT ATAACTTGTG TTAAGACATT TGATTCTGAT 1680
AGCTTTGCTT TTCTCTCCTC CCCTCAATCC CCACCAACTC 1720
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