| Tag | Content |
|---|
EnhancerAtlas ID | HS108-03574 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:182204290-182206610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr1:182204991-182205003 | GCAATGTAAACA | - | 6.07 | | NFIC | MA0161.2 | chr1:182204735-182204746 | TACTTGGCAGA | + | 6.62 |
|
| | 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 |
| GH01I182235 | chr1 | 182204736 | 182205736 |
|
Enhancer Sequence | ATCTGGACTT ATGGTATAAC CAATATGTGG CAGCTGCTAT TACTTTAACT TGTTCTTCTG 60
TATACAAATA ATAATAGCTT TATCTGTTAG GATTCAGTGC AGGAAACAGA AATTGCTTCA 120
CTTACATTGA GTAGGAAGGG ATTTAGTCAA GGGATAATGT GCTTGCAAAA CGGTTAGAAG 180
GGCTGAAGGA GCAGGTTCTA GGCTGGGGCT CACAAAGCAG TATAGAAATT AACCACCACC 240
TCTAGGGCAC CTCTGGAGCT GTGCTGGAAT CCAGAAGTGA CTGCTGCCTC TGCTACAATT 300
CCTGCCTCTC GATACCCAAG AAGCTGGAGA ATGGACTCTG GAACTCTGAT GCAGAAAAAC 360
CTCCTATTTC CCCAGCTTTG CTGGCCAGCA AAATGGCTAC AAAGGGGTGC AGCTTCTGCT 420
TTGCACATCT TGCACTGAGT GCCTCTACTT GGCAGAAGAC AGCTTGCTTC TAGAACCCCG 480
ACTGCAAAGG AGCCTTGGAA TCATGGTGCT CAGCTTTCCA ACTTCACCCA GCAAGAGGCA 540
GGAATGAAGG TTGAGTGACC ATCCACACCA CAGCTGGCAC TTTCAGCTGT CATTGGCCTC 600
ACAGCACCAC AGTTAGGTAA GTGCCCATTT CACAAATGAG GAAGCAGAGC CTTCAGGAAG 660
TTACCTTGTC TGCCCCGGGT CACAGAGGAA GGGGTGAAGA AGCAATGTAA ACAGGTTCTA 720
TCTTAATCAA AGTCTATGCC CTTAACTACC ATTTTTTCTA ATCCTCCCTG CATCTTGAAT 780
GCCTAACTCT GCATGTGGCC ACACCTACTG AATGAATGTT AGAGTTCATT CATCATGAGT 840
TTAAACAGAA AATTACACCA ACTTAGAATG CTGTGGCCTA GAGAAAGTGT CTTTACCTCC 900
TGAGTGCGAC CCAAGTCAGG AGGCAGGAGG CTGACTGAGG GACACGGAGG AGGTATGCAC 960
ACTCACAGCA TGAGGCAGAG CTGTGTGCAC ACATCAAGCA AGGAAATGGG GCCGGAATAT 1020
GGGGCAAAGG CCTACGGATT GAATGGTGGA TTTGGATGTG GGCCACTTCT TCCAGCCCCT 1080
GAAAGAGGAC CAGGCAATGT GGCTATGAAT GGGCCTAATG AGAATTGATT GATTCGCTCG 1140
AGATGTTTTC TTTTTCTTCC TAAAATAGAA AATGACATAC CCCATGATTC ATGCACTCCG 1200
GTGCCCGTGA TAATGGCCTC TTCAGTGCAC TGACTCTGCT GATAACCACA GGCACTCATC 1260
CTCCGCAGAG GGGTTGTGTG CCACACCCTA GGCACATAGC AACCCTGCAG GCTGTCAGAC 1320
ACCTGCCGCA GAGAGTGCTT TCCACACGCT CTCTGGGACA TGAGGCACAG TTCCCAGGAG 1380
TGCCTGAGAA ATCTCAGTTG CCTGGCATAG ATGCTAAGGC CTGAGAGAAG AGCCCAGAGT 1440
CTAGGCCTGA GGGGCTGCAG TCTGCACACA GGAGTTAACT CATACACATA TACAACCCAC 1500
AAAGCCACAC ACATACATAG CACAAATACA CACACAGATA GACACAGCAC ACACAGACAC 1560
ATACATCACA CACACACAGA CACAAACATG CACACTACAC ACATGCACAG CCCACATAAA 1620
CACCCACAGA GTTGCAAATA TACACAGCAC AAATACACAC ACAAATAGAC CACACGCAGA 1680
GAGACACATC ACACATACAC ACAGATACAA ATATACACAC CACACACAAA CACAGAGAGA 1740
CACACACACC ACACATACAA CACACACAAA CATACACACT ACACACATAC ACAACCCAAT 1800
AAACACCCAC AGAGCCACAA ACATATGTAA CACAAATACA CAGAGAGACA CACCATGCAA 1860
AGACCCAGAG AAACACCATA TACCACACAT ATGCACACAC AAACGTGCAC ACCCAACACA 1920
TCACCACGTG CAACACATAC ACCATACACG GAAACACATG AAGACACTTA CGTACACCAC 1980
ACACACATAT ACACACACAG ACACAAACAT ACGCAGCGCA CACACACCAC ACACATACGC 2040
AGGCTCATGC ACATACTCTA CAAAAAGTGC CTCACTACAG GACAGCCATA TCCTAAAAGG 2100
CTTAAAATAA TGGTTATATG GCCTACAAAC GCAGAAGGTG TGTATACAAA CCAGTAAAAG 2160
AAATGAAAGA AAGCATCAAA AATGGTAAAT ACACGAAGAT AAAATCCCTG TTGAAATGCA 2220
CGCATGATAT TTATTGGGAT TGGAGGACAA TTCAGGCAAC ACAAATAATT GATATTTAGT 2280
AATCTTTGGA TTGTTCCTTG TGAACTTATT CAGTTGAACA 2320
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