| Tag | Content |
|---|
EnhancerAtlas ID | HS108-04310 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:227063250-227064640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr1:227063797-227063808 | CCCACCTGCCC | + | 6.14 |
| | | 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 |
| GH01I226873 | chr1 | 227061434 | 227064266 |
| Enhancer Sequence | GGTAAGTGCA GTGACTCCCA ACCTGCTTTT GAACCCTCTT TTTCCATTAG GATTTTCTCC 60
GTGGAGGCAG ATTTCCATGG GAGTTTGCTG TGGCATTTTG AAATCTGTTT CTTACCTAGT 120
TCCATTGGCC TTAAATGTTA AGGCCAAAGC CTTTACATTT CTCTGTAATG AAAAGAAGGT 180
CGAGGAAATT GGGTCATTGG GTTTCCATAA TGATTGCAGG AACTGCTGAC ACAAGCACGG 240
CTGGGGAGAT TCTCTAGGTC AGACTCCCTT GGTTTGGCTA ATTCAGCAGT TTGATCCCAT 300
TCAGCTGATT AATGGGAATG TGCAGTGGCT TCTTTGGATG TTTGATTTTG CATCCTAATC 360
CAAAGCAGCT ATCAGCCTCA GCACTTCCTT GTTGGAAGGC TTTCCAGAAC GTAGTCTATG 420
TTGGACACTT CCTTCTGCCT CTCTGCATTT TCCTGCCACT TCTCTAGAGA ATGGGGTGCA 480
GGGGGTGGGA GACGGGGAAA GCTGGTCGCT GAGTGGCTGA TGGGACTTGA CATCACCCAG 540
CCCCACCCCC ACCTGCCCGT GAGTCAGCCT CCGGGGAGAG TTCATCGCGT CACCGGCACT 600
CTAATGTGGA CAGACACCTA GCAGTGTTGT TTATCTGCAC ACGTTTGGGT GGTGATTTTT 660
CCCTCCAAGG ATTTCAGAGC ACCAGCAGGC TTCAGAGCAG ACTTAGGTGG CTTGCAAAGC 720
AGGCCCTCAG GAATTCAGAG GGTAGCAGAA GTCCATCCCA GATGCTCTGT TTTCCTTCAG 780
GAGCTAGGTA AATCAGAGGG GCTGAGGGAC AAATGAAAAA AGTTACAGCC TTTGAGTCCC 840
ATCTGCTCCT CCTGGCCAAT GAGAGGGGAT CTGGGAGGGG CAGATGTAGA GGAAAATCTG 900
TCTAAATGTT GATGCTCGTT ATTTTCCTTT AAAGAATTAA TAGCCTAAAA TAAACCCTAC 960
AGATACAGTC TGTGTTTATT ATGGCGACTT AGAGAAATGC AGAAAAATAT CAAGAAAATA 1020
AAAACCACTC TTGGTTCTAC CATGCAAAGA TAATCATCTT TAATGTTTTG TAATATTTCC 1080
GATCTTTTAT ATACATACAT TTTATAAGGA CATTCAGATG ATCAGGTTCG TAAAGTTTTA 1140
TGTTCGGTTA AATTTAACAG CGTGTCATTG TTCAGGTTAT TAAATGTTTG AAATAAGATT 1200
TTTGGTGGTC CTGTCACAGT CTCCATGAAG TAGCATTTCA GGATCGAAAG GTATGCTGTG 1260
TTTAAAGTGT TGATTCTTAC TCCTTTCAGT TAAGGCCAGT GCAGTTTGTC CAGGTAGTGA 1320
CTGAGACCCA GTTTTTCCAC ACTCTCCTCC GCAGTGGGCA TTGTTTTGGG CCTTTTTCAG 1380
CCCAAGAGCT 1390
|
| |
|
|
|
