| Tag | Content |
|---|
EnhancerAtlas ID | HS030-01138 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:65932560-65933950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:65933395-65933411 | CTTTGTTTACACTGTG | - | 6 | | Foxq1 | MA0040.1 | chr1:65932581-65932592 | CATTGTTTATT | + | 6.02 | | NFKB1 | MA0105.4 | chr1:65933648-65933661 | AGGGAAATCCCCT | - | 6.15 | | NFKB1 | MA0105.4 | chr1:65933648-65933661 | AGGGAAATCCCCT | + | 6.1 | | REL | MA0101.1 | chr1:65933650-65933660 | GGAAATCCCC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 65932595 | 65932798 | | chr1 | 65933212 | 65933565 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I065467 | chr1 | 65933281 | 65933490 |
|
Enhancer Sequence | GGTCATTTAA GGTCTTCTCT ACATTGTTTA TTCTAGTTAG CCATTCATTC TTCTCACCTT 60
TTTTCAAGGT TTTTAGCTTC CTTGGGATGA GTTAGAACAT GCTGCTTTAG CTCGGGGAAG 120
TTTGTTATTA CCGACCTTCT GAAGCCTACT TCTGTCAACT GGTCAAACTC ATTCTCGTCC 180
AGTTCGTTTC CTTGCTGGCA AGGAGTTATG TTCCTTTGGA GGAGAAGAGG CGCTCTATTT 240
TTTGGAATTT TCAGCTTTTC TGCTCTCATT TCTCCCCATC TTTGTGGTTT TATCTACCTT 300
TGGTCTTTGA TGTTATTGAC CTACTGATGG GATTTTGGTG TAGCTGTCCT TTTTGTTGAT 360
GTTGATGCTA TTCCTTTCTG TTTGTTAGTT TTGCTTCTAA CAGTCAGACC CCTCAGCTGC 420
AGGTCTGTTG GAGTTTGCTG GAGGTCCACT CCAGACCCTG TTTGCCTGGG TATCACCAGT 480
GGAGGCTGCA GAACAGCAAA TATTGTTGCT TAATACTTCC TCTGGAAGCT TTGTCCCAGA 540
GGGGCACCTG CCTGTTTGAG GTGTCTGTTG GCCCCTACTG GAAGGTGTTT CCCAGTAAGG 600
CTACACGGGG GTCAGGGACC CACTTGAGGA GGCAGTCTGT CCATTCTCAG AGCTTGAACA 660
CAATGCTGAC AGAACCACTG CTCGCTTCAG AGCTGTCAGA TAGGGACGTT TAAGTCTGCA 720
GAAGCCGTCT GCTACCTTTT GTTCTACTAT ACCCTGCCCC CAGAGGTGGA ATCTATAGAG 780
GCAGTGAGCC TTGCCGTGCT GCGGTGGGCT CCACCCAGTT CGTGCTTCTT GGCCTCTTTG 840
TTTACACTGT GAGCTACTCA AGGCTCAGCA ATGGCAGATG CTCCTCCCCC AGTCAAGCTG 900
CAGTGTCACA GGTCAGACTG CTGCACTAGC AGTGAGCAAG GCTCCATGGG TGTGGGACCT 960
GCTGAGCCAG GCACAGGAGG GAATCTCCTG GTCTACTGGT TGCTAAGACT GTGGGAAAAG 1020
CACAGTATTT GGTCAGGAGT GTACTTTTTC TCCAGGTACA GTCTGTCATG GTTTCCCTTG 1080
GCTAGGAAAG GGAAATCCCC TGACCCCTTG CGCTTCCCGG GTGAGGTGAT GCCCTGCCCT 1140
GCTTCAGCTC ACCCTCTGTG GGCTGCACCC ACTGTCCAAC CAGTCCCAAT GAGATGAACC 1200
AGGTACCTCA GTTGGAAATG CAGAAATCAC CTGTCTTCTG CATTGATCTC GCTGGAGCTG 1260
CGGACTGGAG CTGTTCCTAT TTGGCCATCT TGGAAGCAAC TGCCCATCTT AGAAACTCTT 1320
ACAGCCAAGA GGAGACTAAG GAGACATGCT GACTCAATGT AATGTGGTGT CCTGGATGGA 1380
TCTGAGGAAG 1390
|
