| Tag | Content |
|---|
EnhancerAtlas ID | HS076-38681 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr22:44658000-44659750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr22:44658949-44658970 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
| | | 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 |
| GH22I044262 | chr22 | 44658661 | 44658810 |
| Enhancer Sequence | TTGGGGTCCT GGCCAGGGTG GGAATTGGGG GAAAAGTTCT TGGGAGCAGC CACAGAGCTG 60
GGCCCTGGAC AAGGCTTGTT GGGACGACAG GGAGGGCACT CCAGGCGGAC GGAACAGCCT 120
CAGCCAAGGT CATTCAGAGG ATCACAAGGA GCATGGCTGT CATGGCACAA GATGCTCCTG 180
GCAGGGGTGA GTCTGCAGAG GCGGCAGCCA CAAAGCCTTC ATCTGCCAGG AGAAGGTGTC 240
TGGACCTGAT CCCAAAGTTG TGGGGAGCCG ACATGGAAGA TCATGCCTAA TTCTCATAGC 300
AGCAAGATTA GGGCTGCAGG GTACTGATTA TCTCTTCTGT GCCGGGCACT GTGCCAAGCA 360
CCTCCCATGC GTGTGGAGCC TCAGTTCTCT CAGCAGCCTC AGGGGTGGGG ACCACTAGTC 420
CCTGCAACTT GCTGATGAGG AAAATGAGGC TCAGAGAGAC AATGTCACTA GCCCAGAACT 480
GCATATCTAG CTAGCAGTGG AGCTTGGCCT GTGCTGCTGA CCGCAGGGCC ACACGGCCAG 540
CCCCTCTCGT CTGGGGCAGT GGCCTGGGCA GGCTGGGGAG TAGCAGGCTG CCCTGCTGGC 600
CCTAGTGGCC CTGGCGAGAG AGGAGCTGAG CCTGGAACCA GGAGCAGGGC CCACGGGGTG 660
AGGAGGGTCT GCAGCTGGCA GGCCTGGTGG GCTGGTGCCT GCAACCTAAG TGGGAAGATA 720
ACAGAGCACC TGGTAATTTG AATAACAATG AAAGCTTCCA GAATGTGGAA CATCTGTGAC 780
AATAACCCTT CCCGCAGACG AAAGCAGAGG AGTCATGAGG CACAACACGC CTCATTCCAG 840
GTGAACTGGA GACAATGTGT TCCCCAGCAG CAGCAACAGC TTCTGTTAGT TAGTTGGTGC 900
TGACGGTATG CATGTGGGGT GTGGGGCTGG GAGCCTTCAC GTATTTTTTT CTTTCTTTCT 960
TTTTTTTTTT TTTTTTTTTG GAGATGGAGT CTGTGTCGCC CAGGCAATAG CGCAATCTTG 1020
GCTCACTGCA ACCTCCGCCA CCCGGGTTCC AGCGATTCTC CTGCCTCAGC CTCCCGAGTA 1080
GTTAGGATTA CAGGCACCCA CCACCACGCC CAGTTAGTTC TTGTATTTTT AGTAGAGATG 1140
GGGTTTTGCC ATGTTGGCTA GGCTGGTCTC GAACTCCTGA CCTCAGGTGA TCTGCCCACC 1200
TTGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACT GCACCCGGCC GCCTTCACAT 1260
ATTTTTCTAA GGGATTCTCA CAGGGACCTG AAAGGGGGAG ATGCTATTAA TCCTACTTTG 1320
TAAATGTGTC CCTGCAGACA GTACAGGGAC ATCAAGGAAC CTATCTGGGG CAAGATGGCC 1380
ATCCCAAGGA ACACTGCCTC AACAAGGAGA AAGAGACTCT GCTGACGCGA TGGAGTTGAG 1440
GGTTTTGGGA GAGAGAGATG AGCCTAGATT AACTGGCTGG GCCTGATGCC ATCACAGGGT 1500
CCTAAGTGAG GAAGGCAGCA GGCTCAGAGT CAGTGGAGGG GATGTGGCCA TGGGAGCAGA 1560
GGTTGGAGAG ATGTCCTTGC ATCTGGAAGG GGCCACAAGC CGAGGAATGT GGGCACCTCT 1620
GGGAACTGGA GCAGACAAGG AAACAGACTC ACCCCCGTGG CCTCCAGCAG GGCCCCGTGC 1680
TGCTGATGCC TTGACATGAA GTGTTCATGA GTCTCCTTTC CAACTGCTGT CCTCTGGATC 1740
TGTACAAGAC 1750
|
| |
|
|
|
