| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01089 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:145389330-145391310 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:145389340-145389361 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAAAAAAAA AAAAAAAAAA AGAAAGAAAG AAAAATTTTT CCTGGCACAT TTCTATCTGT 60
TCCGTTCTGG ATGACTTGCT CTTCAGGCTT ATCCCACAGC TGTTATCATA ATATCTCTCT 120
TTACTGCACC ATCTTGGGAT TTCCATCGCC TCTCTCTTTT GTTAGATCCC CTGCTTCATG 180
GATCTCAAGG GGGTTCATTC TTCACTCACT TCTTCCTTTT GATGATGCAT ATCCTCCAAA 240
ACCTCCTATA AAGTGGTTAC CTTAGAAATA AACTTTTTGA GACACTGCAT GTCTGAAAAT 300
GTCTATTATA CCCATACACT TAATTGATAT TTTACTAGAT AGAGATACAT AGAGATAGGT 360
TGAAATAATT TCTCTCAAAT TTTTAAAAGC ACTGCTTTTT TTTTTTTTTT TTTTTGAAAC 420
AGAGTCTCGC CTCGCTCCGT CGCCCAGGCT GGAGTGCGGC GGCGGGATCT CGGCTCACTG 480
CAACCTCCAC CTGCCGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCCCAG TAGCTGGGAT 540
TACAGGCACC CGCCACCACG CCCGGCTAAT TTTTTAATTT TTAGTAGAGA TGGGGTTTCG 600
CCATGTTAGC CAAGCTGGTT TTGAGAGGAG AGCACTCCTC ATATTGTCTT ATACTTAATT 660
TCTTGTTTGC TGAAAAAGTG GAGGTTGAAA GAATGGGCAG AAGTGAAAAT CGTGGTCAGA 720
CAACCGGGCG CCACATTTCG GGCCTTGTTG TTAAAATTCA ACCCCTGACC TCACCACTTG 780
CGCTGTCTAT AAATTCCAGA CATTGTATAA AAACGCATTA TGAAACTCCC TTTTCTGTTC 840
TGTTTCGTTC TGATTACCGG TGCATGCAGC CCCCAGTCAC GTACCCCTCG CTTGCTCAAT 900
CGATCATGAC CTCTCCCTCC ACCCACAGCC CCTTTAGAGT TGTGAGCCTT TAAAAGGGAC 960
AGGAATTACT TATTCGGGGA GCTCCGTTTC TAGGACGTGA GTCGGCCGAC GCTCCCAACT 1020
GAATAAAGCT CTTACCTTCC ACAATCCGGT GTCTGAGGGA TTTTGTCTAC GACCTCTCCT 1080
GCTACAGTTT CAAACTCCTG ACCTCAAGTG ATCCGCCTCC CTCGGCTTTG CAAAGTGCTG 1140
GGATTACAGG CGTGAACCAC CGCGCCCGGC CCTTGTTGTT TACTGTTTCC CTATAGTCTT 1200
TTTTTTTTTT TTTTTTTTTT TTTGAGACGG AGTCTCGCTC TGTTGCCCAG GCTGGAGTGC 1260
AGTGGCACAA TCTCGGTTCA CTGCAACCTC TGCCTCCTAG GTTCAAGCGA TTCTTCTGCC 1320
TTAGCCTCCC AAGTAGCTGG GACTACAGGC ATACACCACT ATGGCCAGCT AATTTTTGTA 1380
TTTTTAGTAG AGACGGGGTT TCACCATATT GGCCAGGCTG GTCTCGAACT CCTGACCTCG 1440
TGATCCGCCC GCCTCGGGCT CCGAAAGTGC AGGGATTACA GGAGTGAGCC ACTGCGCCCG 1500
GCCTACTGTT TTCCATAGTC GTTTCTGAGA AAGAAAAAGT AACCCTTTTC TGCTCTCAGC 1560
TAGAGCTGGT CTGATAAACA CCTAGGCCAT GATGTTCTCC GGTTCAAACT AAAAATTTCA 1620
CAACACCAAT ATCAGACAAA GCTACCCTCT CACCAAGATG AAAGAAAGAC TATTTCACAA 1680
TCATATTTGA GCACAAACAG AACACTGTTC AAACCATAAT ATGATCAAAC ATTCCCCTTT 1740
CCCAGCTACT AATAGTGACT GTTAATTCTT TTATTTTTTA TTTTTTTGAG ACGGAGTCTT 1800
GCTCTGTCGC CAGGCTGGAG TGCAGTGGCG TGATCTCGGC TCACTGCAGC CTCTGCCTCC 1860
CGGGTTCAAG CGATTCTCCT GTCTCAACCT CCGGAGTAGC TGGGACTACA GGCGCCCACC 1920
ACCACACTCA GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT ATTGGCCAGG 1980
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