| Tag | Content |
|---|
EnhancerAtlas ID | HS108-39421 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:74544540-74545990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLTF | MA0109.1 | chr8:74544605-74544615 | ATATAAGGTT | - | 6.02 | | SPIB | MA0081.2 | chr8:74545734-74545746 | AATGGGGAAGTG | + | 6.18 | | Zfx | MA0146.2 | chr8:74545975-74545989 | GAGGCCGAGGCGGC | - | 6.02 |
|
| | 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 |
| GH08I073630 | chr8 | 74542389 | 74546067 |
|
Enhancer Sequence | GCCTGCCACA TACTCTTACA AAGACAGGAT GTCAAGCAAA CCAATAAGTC ATTCAAACCC 60
AGTGTATATA AGGTTCCTTA AGTATTTGAG GAATCAACAT GGAGAATTCT GAAAATCTGA 120
GACCCACATG GGAGTAAAGA AAGAATGCAT CTTAAGCAAA TTTTACTTAT TGTTCTCTTT 180
GTTATCCTGA AAAAGTCACT CAAGAGAACA AAAAAGGGTT TGCAAATAAG ACCATATAAT 240
CCTATTTGCA GAGGATGACA CTTCTTATGA GACTTAGAAA CCTGCAATAC AATCTGAGCT 300
TATAAGACTG AGAACTCCAA AGCAGGAGAG TGATCAAGAC TGACAAGAGT ATGACCATGG 360
TGATCTCTCA GGAAGCTAAA ATCACCCCAG TTATGCATAA GAAATTCTGG CCAGAAACTG 420
AACACTTCAG AGCTGGTGAA CTCATGATAA AATCAAACAG ATGAAGAGCT AAACTTATAA 480
TCTTAGTTGT CACTTGACTC TTGTTTAATC AAAATGTAAT TCTAATATAA TCAAAATAAG 540
TATATCCTGT TACTTCTCAA ATTTAGAAAG GCCAGACTCC CCTGCAAATG CTTGAGAACC 600
CTGTATTAGA CCTCATAGTT CCTCAACAAA GGGAAAAGTT TAGAGTAAAT GATACGCATG 660
CTATTCCAGG AATAGTGTTC TAGGAAGGCT ACAAAAGGGA CAATTTCTGC TTATACACAG 720
GGAAAAAGGG AGTTGTATTC ACTGCAGCCC TAGTGTATGG TATCCAGCAT GATACCTAGC 780
ACTTAAAAGG AGTCCACTAC ATATCTGTTA AATGAAGGAG AGGTTATAGC TAACAATTAC 840
TGAGTGGTTT ACTATATGCC GGCACTGAGC ATGCAGTAAC TCATCTAATC CTCACAATAG 900
CCTGATAAGG CAAATACATA TTGTTATCAT TTCCATTTTA CAGTTGAGGA AACTGAAAAA 960
CAGAGAAGAT AAGTTGCTTG GCCTAGGCGG AACCAGGTTT CAAATGAAGA TAGAGTGGCT 1020
CCACAGCACC CCCTAACCTC AATACTACAT TACTATATTC CTCTCAACTT AAAAGTGAAT 1080
GATTGCAAGG GAGAGACAGG ACCAGCAAGG GCCAGGTTCT CAGCTATGTG GGAGTAAAGC 1140
AATCAGGACT AGCAGAAGGA CAAGTTCAAA GTGAAAGGAT GCATGTGAGA TCTGAATGGG 1200
GAAGTGCTGG GAGTGAATGT ACTTTGTGAC TATAGACTCC AAGTACCTCT TAACATTGGG 1260
CATGATCTGA CCTTGAGGCG GCTACAAGAT GAGGATGGGC TAGATCAGTG GTTTCATCTT 1320
TGCCTATATA CCGGAAGTAC ATGAGGAGCT TTAAAAAATA CTGAGGACAA GTCAGTAAGA 1380
AAAAGACCAC TGAGGCCAGG CACGGTGGCT CATGCTTGTA ATCCCAACAC TTTGGGAGGC 1440
CGAGGCGGCT 1450
|
