| Tag | Content |
|---|
EnhancerAtlas ID | HS053-27504 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr3:100214120-100216300 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:100215772-100215793 | TCTCAGTTTCTCTTTTTATTT | + | 6.92 |
| | | 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 |
| GH03I100496 | chr3 | 100215136 | 100216325 |
| Enhancer Sequence | GAAGGGCTTG CGTTTCTGGG AATGGGTTTT GTCAAACAGT TCTGGTTTGG GAATGGGAGG 60
AAGGGAAGGG ATTATAGAGG AGCAGGAACA TTTTAGGAGG AAGGAGACCT TTTGCAGGGG 120
CAAAGGCACT ATGGCTGGAA AGTGAGGAGC TATCCTGTGG ATGTTGGGAC ATTGGGATAA 180
TCTGTGGGAG GTTAGTTGGA GGAAAGTTTG GAAAGGTGGG AGAGGTGGGA AGGGACAGCA 240
TAAATTACCT GATAAGGAAA GAGAGGCTTG GGAGGTAGAT TGGTGGGGAG ATGGCAAGCC 300
GAACTGTCAG CAGTTACACA GAAGAGGTGT TTCTGGAATA ATCCATCTCT GGGGTCCTGT 360
CTTCTCTCTT GCCCAGCATT CCCTTCCCAT CTGCTCCACT GCTTCTATAA CCTCCATCCA 420
GGTCCTGCAG GTTGGGTGGG TAGGGATGGG CAGTGAGTCT GTGTTTTGGA GTCATTCCAT 480
GGTGGCTGTC TTGGAGCTCT GTTTAAGTGG TCTGGTGCTC AGGGCAGTTA CCCAGGCTAC 540
TTTTTGTTAA CAGGCCATGC CCTAAAATCT TTGACATGGA TGTGATTGTT ACAACCCTCC 600
CCATCCGCAT ACACGCCCAT AGTGTATGCC GAGTAGCTCT TTCTCATCCT GCTGATAGAA 660
TCATCTACTC ACATTTTAAC ACATATAACT TCATAACTTA CAATTATTGA AGTAGATAAG 720
AACTGTAATA TGCACTTAAG TGGAGAGTCA CTTTGGAGTT CCCTTGCTTT CTCTTCCCTG 780
AGAGCATTGT TCTGTGGTAG AGAGGTGTGC CTGATGCTGC TGTTGACCAC CTGTGTGACT 840
TCAGGCAAGA CATTGAACCC TTGTGGTCCT CCTTGCCATC ATCTGTGAAA TGATCTCTAG 900
AGGCCCTTTT TCTCTCAGAT AATCATTTAT TCTTCTCCCC GGATCCCTGG AACAGTCCAT 960
TATTCACAGA TGCCTATTTG ATACATCTGC GACTAATATT TTCTGATCAC TTAATACATG 1020
GAGAACGTTC TGATGATGGT CATGTCCTCC TCACATCCTC CTGTGAGGGT TGGTACCTAT 1080
TTGTGTCCTG TTTTTCTAGT TGAGGAGACA AGGGCAAAGG CAGTTTAAGA AATTTGCCCA 1140
AGATTACACA GTGAACAAGT GGCAGGTGTA GAACCAGTCT AACTTTGTAG CCCGAGCCTT 1200
ACCCAATAGG CTATGCTACC TTAGGTATAA TACAGCTACA GCTGCTCTTC GTGTTTGTGG 1260
TGGTGATAGT TGAGAAGTAC ATGGAAGGAA GATCATTGGA GAAAGGGCAT ATTTGGAGAT 1320
ATTGATTTGG TAAAATTTGC CTGGCGGGGG CCAGAATATC AATGTGAATC TTGTCTATGA 1380
AATGTGCTCC ATATGGAGAC AGGAGACATG TGGATCTCAT TGCAGGCATG CACTCTGTCT 1440
TTTCACCTTG TTTGAACAAA ACCCACATAG CACCTGGTTG TCTAGCAGAC ACTCAATACA 1500
TGTCAATTGA ATGACTGTCC CCTTTGAAAA AGGAAGTTGT GACCACACTA TTTTTATTTA 1560
AAAAAATAAA TAGAGAGACT ATGAAATGTC CCAAGACTTG TGGGAAAATG GGTCAGATGC 1620
CAGGTAAACA TTCTACTTCT GCTTTTGGGG CATCTCAGTT TCTCTTTTTA TTTCTGGACA 1680
TGCTGTGGTT TTGGGCTAAG AACTTCTCAT GGTGAATATC AATGAAGGTC TATTTTAGGT 1740
ATATAGTTAT TAATCATACC CATTCTGGAT TTGGCATCTA TCTTTTTGGG AATTCATTCC 1800
TTAAATATTT TGTGTATTGA ATCAACTTTA AAATATTTGA AAAATGTTTT AGGTTGCTCT 1860
TTATCTAATG TAGTTGCTCT TTTCAGTATG GCATAGTGAC TAAGCACACA GGCTTTGAAG 1920
TCAGACTGTG AGGGTTTGAA TTCCAGATCT GATTCTTACC AATGTGGCCT TGAGCAAGTC 1980
ACTTTCCTCT AGAAGCTTTT ATTATCTGTA AAATGGGGGT ACTCATATGC ATTACATGAG 2040
AAAAGCCATG GAGAGCATTC AGTATATTGT CTGGCTCACA GTAAAGCCTG TACATGTAAG 2100
CAATTCCTTT TTTATTGTGG TAAAATATAT AACATAAAAT TTACCATCTT AACCATTTTT 2160
AAGTATACAG TTCAATGGCA 2180
|
| |
|
|
|
