| Tag | Content |
|---|
EnhancerAtlas ID | HS059-04142 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:217200390-217201410 | 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 | chr1:217200915-217200936 | AAACAGGAACTGAAACTGCAA | - | 6.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAAGATTGG CTGAAATGAT GTATCTTTAA AGGTAAGAAT TCTAAATGTT CTGTGTCGAT 60
TTTGTTTTAA ATCTCTCACC ACAAAGGCCA CATGTTCCTT CTGTTCCCCA AACATACTGT 120
CCCCAAGAAC AACTTCCTAA TGTCTATAGT AATTCCAGAA AAGCCACAGA GAATTACTGT 180
CTCCAGTAAC CAGAAAAGAA TAAATACATC CTGAACCCAC ATTATAAATA GAAATAGTCA 240
CTAATCTTCT GCTCAATGAC AAGCACCCCC TTAGAGAAGA CCAGCTCACC AAAACTCCAC 300
TGAATTATTG TCCTCTTTCC TTACACCCTA GTTCTTCGTT ACATGCATTC TTCAGCCCTT 360
ACAAACCACC CTTACAGAGG TGATTCAGTG TAATTAGAAA TCGAGTTAAA TCTTAGGGCC 420
TGGAACCTCT ATTTCTTCAT AATGTTGTAC ACTTAATTGC TCTTGCCAGT TAGCAACACA 480
ATTATGTTGT CTGGAAATGG AGACAAACAA TAGATTTTAG TATTTAAACA GGAACTGAAA 540
CTGCAAGCAG AGAGCCGCAA ACCACACCAT TAAACTGGAA TTAAAGCTAT ATGTGAAAAG 600
AAAAAGTTTC ACTCCCAGCA ATCATCAGCC TACCATGCAA AAAGAAACTA CCCACAGATC 660
AGAAGGAAGG TGGAACACAG GAGGTAAAGC TTGGGTTCCT AGTTTAGGAT GGGATTTTAT 720
GAAAACCCCA GGCATAAAAA TATGACAGGA TAAAGTAGAC AAATAACAAT GCAGGACAAC 780
ACTTGACCTT TAGTGGTTAA ATGAATAAAA GAAGCCTCTG TATTAAGAGT ATCCCTTGTG 840
CATAATCATT GCCTCAATGC AGCCTGTCCC CAACCTCTAT GCCTACCAAG ATTTTCTAAA 900
CTAATGCCTT ACTAACAGGG TTAGAAAAGA GAACAAACAA CAATCAACTG AAATTCATTC 960
CATTTTCTAG AAACTGTCAC GAGAATCACA AAAACTCAAG TGGCGCACAG ATTTGGCCTT 1020
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