| Tag | Content |
|---|
EnhancerAtlas ID | HS091-01304 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:38379920-38382250 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:38380446-38380457 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr1:38380446-38380457 | TTCTTATCTGT | + | 6.62 | | IRF1 | MA0050.2 | chr1:38382066-38382087 | TTTTTCTTTTTCTTTCATTTT | + | 6.89 | | IRF1 | MA0050.2 | chr1:38382072-38382093 | TTTTTCTTTCATTTTTTTTTT | + | 7.51 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I037915 | chr1 | 38381121 | 38381270 | | GH01I037916 | chr1 | 38381481 | 38381630 |
|
Enhancer Sequence | CTCTGTCTAT GGAGTAGCCA TTCTTTATTA CTTTACTTTC TTAATAAATT TGCCTTTACT 60
TTACTCTATA GATTCGCTTT GAATTCTTTC TTGCTCAAGA TCCAAGAACC CTCTCTTGGA 120
GTCTGGCTCG GGACCCCTTT CCGGTAACAA TTTTTGGAAC AAAACCCAAA CCTCTGAGGA 180
TTGCATGAAA AGATCTTTAT AAATAGCTTC AGACTTCCTC TCCAGCCCCA TTTCCCATCC 240
CCACTGGAAG CTTCTCTCTC TTACCTCCCA ATCCAGTCAC ACCAAACTTA CCTTTTCACA 300
CACTGCCTAT TCACTCCACC CCTGATCCTG GGTATATCTT TCCATATCCC AATTCCACCT 360
TCACGTGATG AACTACAAAC TCATCCTTCA AGACTCAGTT CAGGAGTTAT CTTCAAAAAA 420
CTTTCTCTGG CCCCCTCCAT ACATTCTCAC ATAACTCAGT GCTTACTTCC ATCAAGGCAT 480
GATAATGGTT CCATTATGAT AATGGGATCA TACCTGGGTT TAATTGTTCT TATCTGTCTT 540
ACCTCTACAC CTAGACCACT AGCTTCTTGG AAGCAGGGAC CAATGTGCTA TCTCTGGCCC 600
CAGCTCACCA CAATATATGG CACACACCAG GCAGTCAGTA AACACACCCT AAACAAACAG 660
TCCCCAGGCA GATTAAGCTC AGTGTGATTT TTCTGTGTAC TCTCATTGAC CACCTTTCAT 720
GCCGACAATT GAAACCATTT CCCTAGGAGC AGCCTACCTA GTAAGTCAAC AAGCTACAGT 780
AACAACTGCA GCTTGATTGC GATGTGTAAA AGTGCAAGTG TTCTATTTTT CTTGCAAATT 840
CTGTGCTTTG TACTGCATAT TGTGTAGAAC CAAAACTCTC ACATGCCTCA CTAAATAGAC 900
AGTGTTGACC CTTGAGGTGC CTTCCTCAGC CCAAGCAGCA ACATAGCCTA ATATAGACCC 960
ACAAGCCCTT ATCTGAAGCC TCTTGGGCCA AGTGCATTTT GGAATTCAGA ATGTGGGAGA 1020
TTTTAGGAAG ATAACACATT ACCTGTATCA AATACTACAT AACAACCCCA GCAGGGTCTG 1080
AGGCAATACC CAGTTAATCA AACGCTTTCA TATTTCCACA GTATAACTTA CGAAGAGTAA 1140
TACTTAGTGA GAGAAACAAA GCCTATAAAT AGTCTCATGT CAGTTCAAGC AAGTCTTACT 1200
GCCAAATTGA GCTTGGGTCA AACTTACAAG AAAAATTTGT TCCAGCCTTC AGAGCTTTCA 1260
GGACTTCAGA ACTGCTGATA AGGGATTGAG GATGGTAGTT AATGAGCATG GCCTGACAAT 1320
ACCTATATGC ATTAGAAAGG ACTGGAGTAT ATGTCTGTGT GCATAGATAC CACACTTATA 1380
AATATTCACA TATGCTGTAT TTGTATGGAC TCAGACACAG ACACATGGAA AGTCTGGAAG 1440
GGTGCACAGC AAAATGTTAA CAGTAGTCAT TTCTCAGTGA TTAGATTTCT TTTTCTTTTT 1500
GCTTATATGT ATTTCCTATA GTTAGCTATA ATAACATGTT TTTTGTGTTT TATATACATA 1560
CACAGGCTTT GGAGTCAAAG ACACGTTATA TTGAGAAAGT TATCTAACTT CTCTAAGCAT 1620
CTGCTTCCTC ATGTGAATAA GATAACAGTG TCTGCCTCAT ACAATTGCTG TCTTCTTTTC 1680
CCATAGTTAA CTTGAGGGTA TCCCTCACTG CATGACCAAG AGGTGTTCTA GAAGCCAAAT 1740
AAGATCTGTT GAAGGCCCAG ACCTATAAAA CAAAGATAGG CAGCAAGGCC TTGATTTTAA 1800
CATCCGGTAG CCAGGCCTAC CACTGAATTG GTGTCTGGGT TTTTCTTTTT CCTTTTTTTT 1860
TTTGAGATGG AGTCTCGCTC TGTCACCCAG GCTGGAGTTC AGTGGTGCAA TCTTGGCTCA 1920
CTACAATCTC TGCCTCCCAG GTTCAAGCGA TTCTTGTGCC TTAGCCTCCC AAGTAGCTAG 1980
GATTACAGGC ACCCACCACT ACACCCAGCT TATTTTTGAA CTTTTAGTAG AGATGGGGTT 2040
TTGCCATCTT GCCCAGTCTG GTCTCGAACT CCTGACCTCA AGTGATCCGC CCACCTCGAC 2100
CTCCCAAAAT GCTGAGATTA CAGGCATGAG CCACTGCAGT CTGGGCTTTT TCTTTTTCTT 2160
TCATTTTTTT TTTTTTCTTT TTTTTGAGGC AGAGTTTTGC TCTTGTTGCC CAGGCTAGAG 2220
TGCAATGGCA CGATCTCGGC TCACCACAAC CTCTGCCTCC CCGGTTCAAG CGATTCTCTT 2280
GCCTCAGCCT CCCGAGTAGC TGGGATTACA GGCATGCGCC ACTACGCCCG 2330
|
