| Tag | Content |
|---|
EnhancerAtlas ID | HS092-30558 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr4:114961410-114962710 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr4:114962454-114962465 | TGCTGAGATTT | - | 6.32 | | IRF1 | MA0050.2 | chr4:114961710-114961731 | AACTGGAAAGTGAAACTAATA | - | 7.39 | | IRF2 | MA0051.1 | chr4:114961714-114961732 | GGAAAGTGAAACTAATAA | + | 7.99 | | Myog | MA0500.1 | chr4:114962508-114962519 | CTGCAGCTGTT | - | 6.02 | | RUNX1 | MA0002.2 | chr4:114961944-114961955 | AAACCACAGAG | - | 6.14 | | Tcf12 | MA0521.1 | chr4:114962508-114962519 | CTGCAGCTGTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACAGTAAAG AGAATAGTAT AATGAAATCC CATTACCCAC TATCAAATTT AAACAATCTG 60
AATCACAGAA GTAACTTTTT TCTATCATAA TTTCACAGAA CTTGAGAAAC ATTGGGCCTC 120
AAAGAGATCA GCCTGGTAAC AATAACAGTA TTTTGCAGAT GTGGCGGTTG AGGGCTAACA 180
AAATTGAGGG AGCTGACCAA AGTCACTCAG TAGCAAAGCC AGAAGTAGAA ACCCTGTCTT 240
CCAGTTGACA GCTTAGCAGC ATAAAATATG CAAACTTTAT TTTTGATTTT CAGTTTTTTA 300
AACTGGAAAG TGAAACTAAT AATCATAATT TACAGTGTTG CTTTGAGTGG AAGCCATGTA 360
AAGAGGCTAG GTCCTTTTCT GGAAAGTAAT AGGTCATCCA AAACATAGAT CCCTTTCTTT 420
CCTTCCTCAC TTATCTCTAG CATCTGTAAC CACACATGGT AAAAACCACT CTGTTCAGCC 480
TGGGAGGCCA CCCTGAAACA GAAACTTCAG CCCTGGGTGA AAAGCCTCTA TCAGAAACCA 540
CAGAGGTTAG GAGGGAAGGT GGGAAAGCAC AAATACCTAA GCTCAGAAAA GAAGGCGAAA 600
ATGTTAACAG TTGGCCTTCT GTCCAGAGAG GCAATGGAGT GGACAGTGTA CAGCCAAATC 660
CCCAAATCAG GCAGCTATTA ATATATGAGC TAGACATCCC ACAAGTCACA CTTAGGACTG 720
GGGCACTGTT CTGGTTTGTC TTAGGGATCT GGATCTCTGG ATTATGAGTA GAGCAGAGCT 780
GATGAGGTGA GTGACAAATA CTGAAAGGGA ATTCATATGT AAGCACATTA AGGAGAGAAA 840
CGAGAGGCAG AGGCTAAGAT CAAGATCAGA GATCAATTTT GCCCCGATGT TTGTTTCTTA 900
AATGCCAACT AAAATAATTT TGGAATTTAA TTTATTGCCT CTTTGTTTAT GCATGAATTC 960
TTTATGTAGA TGTCAGGTAA TAGTGTAACA TCTTAGCAAT TTGTGAACAT ATGGAAACCA 1020
ATGACTCTGT GTTCTTGGAA TCTCTGCTGA GATTTTTATC TTGTAGCATG GACAAAGATC 1080
CCAATCAATG GGCATTGCCT GCAGCTGTTA CATGCATGTA ACAATCTACT TTTATTCAAG 1140
CGTACTGGAA TCATTTGTCC ACTGACTTCC TTTGAAGAGT GAAATGAAAT AATAAGTTAT 1200
AGTTAATGTT TCTGTTATTA AAAACTCTGC CTTTTAATGT ATTAACTTTT TTTTCTTATT 1260
AAAGTGCTTA TTAAGTAATA ATCTCTTTGG CCTGGCTTAC 1300
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