| Tag | Content |
|---|
EnhancerAtlas ID | HS026-01845 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:101048180-101049360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:101048693-101048708 | AGAGTGCAAAGTTCA | + | 7.66 | | MNX1 | MA0707.1 | chr1:101049047-101049057 | GGTAATTAAA | + | 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 |
| GH01I100582 | chr1 | 101048131 | 101049270 |
|
Enhancer Sequence | GTAGTAAGTA CTCCACAACT TGAGCCAGCT TCTACATCAA CCACTTGGCT TCGACTCCGT 60
GTAAAAAAAC CCTAGACATC ATGACTATAT AACCTGAGAG AATCTCCATA TCTAGGTGTG 120
TGGATTCTAG ATTTTTATTT CAAAATAATC TTGGGCACTT ACTCCCTGAT ACTGGGCTCC 180
TTCTCTTACC TCACCCCACT GATCCCTGGG CCCAGGCTAC TACAGTTGCC TCATGTCACA 240
TACAATCTGT GCTTGCCTCT GTTTAGGAGG ATGCCAAAGA CCATTAGGAC CTAAATAAGG 300
TTTTCTTATT AAGTAAGTAA AAAATTGGAA ATAAAGAAAC ATTGGAGGGA AATCTGAAGT 360
TTTCGTGTTG GGGAAGGACT GCTTCATTTC TGTGCTTCTC TGGACCCTTT CCTCTGAGAT 420
GGGGGAGGTG AACCTGAGCC TCACGTTTGT TTGGATTGTG AAGCCCCAGG GGCTTCTGAA 480
CAGACTGTTC TTGATTCTAA GGCAGGACTG CTGAGAGTGC AAAGTTCAGC CTTAAAAATA 540
ACATCTCTAT CTCTCAACTG GGCAAAGGGC CTTGCACTTT GGAATGAGAC AAAAGGTAAC 600
CATGGGATTT TGAACTTGAG CAAAGAGAGG GGGATTGTGG GTTCTGGGAA GCTGCTTTTT 660
TGGGGCTTTT TTTTTTTAAA GGAGAAAAAT TGACAGTTTA TAAATTGGCC AACTTGCTAG 720
CAGATAATCA GTTATTATTG TCACTTGTAG ATAGTGTCTG GCAAAATAGA GAGCTGGTAA 780
GAACTAATGA TTGCTAGGGA CTCTGGAACC AACCTGGTGT CTCTCCCTCA ATTTCTTTTC 840
ATTTTTCACA GAGCCCATTT CAATTAAGGT AATTAAAAGG CTATTATAAT TTGTGAAAGC 900
CTGGGCAAAT TATTTATATT TCTTAGTCAG TTTCCTTTCT GTAAATCGGG GCTAAAGGAG 960
CCTTGATGTG AGAAATAAAT AAGATCTGAC TGTAAAAACC CTGACACATA GTAGGCATGC 1020
CATAAGTGCT AGTGCCTTCC TCTCTCCATC TCATTTATTG GCTGACTTCT TTATTCCTTT 1080
CTCTAGGTAA AGACTGACAG GTGGAAAGGA AGTAAGAATG ATATGAGGAA GGTCTACCTA 1140
CTGATTTGTC CCGATAAAAG AGAAAGATTT ATTTAATAAA 1180
|
