| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00495 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:28305510-28306670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:28306314-28306333 | GACTGCCATCTGCTGGAAA | - | 6.59 | | NFIC | MA0161.2 | chr1:28306415-28306426 | TACTTGGCACA | + | 6.32 | | Nfe2l2 | MA0150.2 | chr1:28306249-28306264 | CAGAGTGACTTAGCA | + | 6.35 | | STAT1 | MA0137.3 | chr1:28305791-28305802 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr1:28305791-28305802 | TTTCCCAGAAA | - | 6.32 | | Stat4 | MA0518.1 | chr1:28305788-28305802 | TCATTTCCCAGAAA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 28305641 | 28306639 | | chr1 | 28305616 | 28305920 | | chr1 | 28305951 | 28306585 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I027979 | chr1 | 28305616 | 28306712 |
|
Enhancer Sequence | CTTCACGTTG AGGGTGAAGT CCCTAAGATC TTAGTGTGAG GGAATTTCTA TAAATGGGAA 60
AGATTAATAG GTTTAGTGAC TTGCCCCTAG ATCACAAACA AGCAAGTAGC TAGAACTTGG 120
GGCCCCTGAC TCCAAATCTA GGCTCTGGTC ATTGTGTCAT AATGAATGAA TGATTTTTGG 180
GGTGAAATGT TTTAGGGTAG AAAAGAGAAG TGAAAACACA AGGCCCTGAT TTCTTGTTAG 240
AAACAATAAC AAACAAAAAG CCATTTCCCT CCAATTCTTC ATTTCCCAGA AACAGTCCTG 300
GGTATAGGCC TTACGTCTTT CAGTGAGAGA ACAGCCCCAG AATAGAACTG AGAACAGTGA 360
CCAATAAATA TGGCATCAAC ATTTGTCATA TCTGGAACCT CCTTACTTAC TATACCTTGT 420
AGTTGTAACC AAGATACTGC ATCACTGAAA TTGACCTTGG GAAATGGGTG ATTTAAATCC 480
ATTTCTCAGA ACTGCAGACA GTTTTGAGAA ACATGGCAGT GTATCAAAAC TCAAATCCCA 540
TCTGCAACCA ACACCTAAAA CATACACAGA TCATACTGCT GTGGGAAAGA TACTTTATTT 600
GTATAAATAA AAAGAAGTTA TATCCCTTGC TCTTTTTATC TCCCTGCTTC TGCCACCTTC 660
TTCAGTTAAA CAAGGTCCTA ACTTTGGCTT TCTTCTTCAT CCTGCTCTAT TAACCTTCTT 720
GTTCTTTCCC CTTGCCCAAC AGAGTGACTT AGCACCAGGG TTCCTGTGTA AATAAGATAA 780
AGCTGCCTCT TCCTCAAGAC ATTTGACTGC CATCTGCTGG AAAATCACTG TAATATATAA 840
ATATACAAAT CTAAGATAAC TGTAACATAA TTGGCCAGAA CTTATACTTC CATACGCAGA 900
AGTCCTACTT GGCACAGAAG TTGTGCAGAT ATGTAACTGC AAATCTTTGA CATCCTTAAC 960
CCAGTGGCAC TTCAAAACAG ACGGACTAGT CAACTGGACC AGACACTAGA TCACTCTGGG 1020
CTCAGCTGGC CACTTACAAT ACAAGGCTTG GCTTAGGTGC ACTTGGGTCT CTTTTAGTGC 1080
TAATATTTTA CAATAGAATT GTCATGCCTT ACATTCATAT GAGGGATTCA ATCAATGTTT 1140
GCTGAGTAAA TTCATATTAA 1160
|
