| Tag | Content |
|---|
EnhancerAtlas ID | HS104-58757 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr8:104292840-104294250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLF | MA0043.2 | chr8:104293394-104293406 | TGTTATGTAATG | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 104293137 | 104294009 | | chr8 | 104293808 | 104293984 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH08I103280 | chr8 | 104293147 | 104294163 |
| Enhancer Sequence | AGGCTGAGGC AGGAGAATGG ATTGAACCTG AGAAGTGGAG GTTGTAGTGA GCCAAGATCA 60
CGCCACTGCA CTCCAGCCCT AGGCAACAGA GAGAGATTCT GTCTAAAAAA CAAAAAAGGA 120
AGCACTGTCA AGACATGAAG AATAATTTGA GATCACAACA GGAGATGGTG AGATCACAGA 180
AAACATATCC AGAATATTAT TATCCCTTAA TAATAATGAT TAATAGCTAC CATTAACTGA 240
GTGTCCAGTA TAGGCCTGGC ACTTTATATT TGTTATTTTA TTTAACTATC ACAATCTCCC 300
TGTGAGGTAG GGATAATCAT ACCCATTTTT TAGGTGAGGA AACTGAGAAT TAGAGAAATT 360
AAATAACTTT CCCCAGTCTC ACACAGTTGG CAGATAGTAA AATGAGGCTT AAATCCAAAT 420
CTAAGTGACT TGAAACCCCA CACCTCACTT ACCTTAAGAT GCATTCCTGA CCCATGGAAA 480
CTGCTTAATA TATATTGAGC ACATGAATAA ATAAAGGACC ATGAATAAAC AGTGGCTGGA 540
ATGGAGCATG TATCTGTTAT GTAATGCCCA TGTTGGCCTT GATTAGAAGC TCTTAAAAAC 600
AAATGAGTAA CAAATACATG TTTTGTTTTG CTCCAAAAGG TATAACTGGG ACAGATCAGT 660
GGAAATTGCA GACTTCCTGT GGCTTCCTGT ACAGGAACCT GGCTTCAAAG AGTCCATTGC 720
CTGAATGACC TTCAATTCTG TGATTCAGAG ATTCTGTGAG AGTCTGTGTC TCTACAGAGG 780
GATAATAAGG GAAAACATTC CCACAGTGAG AGCTGCCTAG TAAAACAGTG AGCTACCCAT 840
TTTGGAAGAT GTTCCAGGTA CATGACTACA TGCCAGAAAT GCTGAATAAG AAATTATTAA 900
ATTGTGTGGT GTAGAAGGTT GTTTGGAAAA TGGCTGCAGT TATTCCCTTT CCTTTATTCA 960
TTCTCCTTTG CAAGATGACT CTTAAGCTCC TCCCATTGAG AGATGGTATT TCCCCAACCC 1020
TTGAATCTGT GTTGGCCTTG TGACTGGCTT TGCCCAAAAG AATGCAGCAG AAGACATTTC 1080
ATGCCAATTC TAAGTCTAGG CTTCAAAAGG CCTTGCATAG TTTCAATCTC CTTTTTGAAA 1140
CCCTGAGGCT GCCAAGTGAA CAAACTGTAG CTAGACTAGC CTGCTGGAGG ATTAGAGGCT 1200
ACATGGAAGA GAATAGAAAT GTCCCAGTGA ATAGTTAGCT AACCTCTAGA AGCAGAACCA 1260
CCTAGCTGCC TTGTAGCTCA CCACATATTC ATGGGCAAGC TCAGTGGAGA CCAGAAGAAC 1320
CAACTAGTTG ACCCATAAAC TCAAGGGCAA TAAGAAATGG TTGCTGCATG ATTCTCATAA 1380
GCACCTCCTG ACATGAAGGG AAGATAAAAG 1410
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