| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22758 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr7:66223040-66224660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr7:66223976-66223987 | ATGTTACATAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 66223384 | 66223719 | | chr7 | 66223156 | 66224400 | | chr7 | 66223934 | 66224293 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I066757 | chr7 | 66222789 | 66225186 |
| Enhancer Sequence | TATCGTTTTA CTAGAATTGA TTGGATGTTT CCTGTAAGTC CCAGATGAGT TGCCTGGAGA 60
GAGGAATGAC CTCTGAGGGC ATGACATTGA ACCCAGGAAT AGGAAGCGGA CCGCCAAGAA 120
GGATAGAGGG AAACTACTCA CATCTGCAAA GTATTTTCGT TTTGCTTTTC TGAGACGAAA 180
CTGGTTTGCA TCCAGAGCCT TAAGAAAGAA CACTAATAGT TCTGTGAGCT TTGTAAGTAA 240
GCTTTGTACC TCTCTGTCCT TTTTAGGGTA CCTGGACCTA GAATAAAACC TAGCGCCGAG 300
GCACAATTTA CAGAATCCTA ACTGTCCCAG CAGCAGAGAT CATTTTTACT CTGTCTTCCC 360
TGACATAAGT GGGACCAATT GAATTGTGCA TTCTTTATGC CCAGGTTGCT CAACCAAGCT 420
TCTATTTATT GGAATGCAGT GCTCCAACAG GAGCGATGTG TGGCCCCTCG GAGCTCCCTC 480
CTGGAAGCAG TGCTGGTGGT GGTTACTGTC TAGGGACAGG TCTGTCTGCC CAGGAGAGAA 540
GGAGTTGAGT CTCACGCAGC TGATCCCCCA TGTTTCTTCC TGTGTTTACA GGATATGCTG 600
TCTGTAGCTG TGATGTCCAA TCTGGGTGTG CCGACTCTCC TGCCTTCTAC CGTAACAGCT 660
GTCACCACCA CCACATAGCC TTTCAAATGA TGGCACTCTC TTTTGGTGGT ACCCTTGCTC 720
TCTTTTTATA CTTAGAAGCA GCAGAATGAT CTGAGTGTTG TGTTTAACTG GTACACATTA 780
GTCCCATGAT AGGTGTTATT TTTATTAAAA AACGTTCATG TGTGATTTTT AACTAAACTT 840
TAAAATTTGG AACAATTAAT GACTTCAAAT CCATAGGAAG CTGTAAATAC AGTACAGACA 900
GGTCCTGTGT ACTCTTCTAG TTTGCCTAAT GGTTACATGT TACATAACTA TAATGTAATG 960
TCAAAACCAG GAAATTGATA TTTGTGCAAT GTATGTGTAT AGTGTCATGC ACATTTCATC 1020
TCATACGTAG ATTCCTGTAG CCACCACCAT AGTCAAGATA CAGAACTATT CCATTACCCC 1080
AAAGACTTCC CTTATGACTC TGTAGTCACA TCCTGTGTCA GCAGTCCCCA GGGCTGCCCC 1140
CAGGTTTCGT AATTCGTTCG AGGCTCTCAC AGGACATATT TATTCCTTGC TATGGTTTGT 1200
TACAGTGAGG GGATACAAAG TAGGATTAAT AAAGGTTAGT TGTGCATTGA GCAGATTCTA 1260
CAGGACACCA GCATTGTTAA GATTCGAAGC GTCTTCTCCC AGCAGAGTTG CCCAGGATGT 1320
GCTTACTTCC CCAGCCGTAA ACTCTAGCAA CATGTGTGAA GTGTTTTTTA TTGTGAAAGC 1380
TCATGTACAC CTCAGAATCC AGGGCTTTTA CTGGAGGTTG GTCACATAGT ATATTAGTTC 1440
GTTCATTCTC ACGTAGTTAT AAAGAAATAC CTGAGATTGA GTAATTTATA AAGAAAGGAG 1500
GTTTAATTGG CTCACAGTTC TACAGGCTGT ACAGGAAACA TTGCAGCTTC TGCTTCTAGG 1560
GTGGCCTCAG GAAGCTTCCA GTAATAGTGG AGAGCAAAGG GGGAGCAAAG TGTCTCCCCT 1620
|
| |
|
|
|
