Tag | Content |
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EnhancerAtlas ID | HS185-00390 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:85794180-85795260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:85794687-85794708 | GAATTGAAAGAGAAAGAAACA | - | 7.01 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_02338 | chr1:85793006-85798614 | Astrocytes | SE_35266 | chr1:85790947-85798610 | HeLa | SE_37476 | chr1:85793138-85799262 | HSMMtube | SE_37964 | chr1:85789961-85801615 | HUVEC | SE_39280 | chr1:85792961-85798232 | IMR90 | SE_44427 | chr1:85792983-85799323 | NHDF-Ad | SE_44926 | chr1:85793440-85798600 | NHLF | SE_45615 | chr1:85789836-85801531 | Osteoblasts | SE_47178 | chr1:85790694-85797488 | Panc1 | SE_51850 | chr1:85793492-85798592 | Skeletal_Muscle_Myoblast | SE_63644 | chr1:85793492-85798696 | HSMM |
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| 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 |
GH01I085325 | chr1 | 85791158 | 85798973 |
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Enhancer Sequence | GGGATTCCAC TATGTCTAAA TCTCTGTTTA TTATGTGCTG TTGAGGGTGG ACCAAGATGG 60 CCAGTCTGCT CATGTTTGCA GTCAGAACTG GACGGTCATC CTGTCACATG AATTGGACCT 120 AGTTTACCCA AGAAGTTCAG AATTTCTTCC AGACAACTGG GGAGGCAGTT CTCTGAGCCA 180 GAGGTTTACT AAGTAGGACC CCAGTGGTTT GAGGACCTCA GAGAGATCCT TAGAACATGT 240 ATACACAACC ACTGCTACCT GGTCAACCTA GACACAAACA AAACAAAATC TAGAAAATCT 300 ATTACTCACA TTGACTTACT TTTCTAAGCA ATTGGGAAAA CTGTGTGTGG CATATTTTGG 360 CCCACACATT CAGGCTAAGT GCTCCCACCA CTCATAATCA CCAGATAACT GCCAGTTGGC 420 TTTCCATTTT AATTTGTGAT CTGCAGAAGC TTCATTGTAC TCTTTACCCA CAGATAAATA 480 AATCACCCAT GTCTCTTAGT ACCAGATGAA TTGAAAGAGA AAGAAACATG GCAAGACTAC 540 ATCTCTTAGG CCTGACTTTA TTCACTGGAT CTAGCGGTCT GGGCAAATTC CCCACCTCTC 600 AGTGTGACTC ATGCATGTCC GGAGGTGACT ACAAAGCAAA AGCATGGAAT GTCATACATT 660 CCAGAGGAAG TGTTCTCAGG GATTGTTATC AGTGCTGACT TCTTGTTTAC CAGTGAGGAA 720 ACAAACTAAA ATCTCCAAGG TTGTGCCCAT CTCAGAAAGT ACCACGTGTC ACTGAAGTGA 780 CAGGGCCTGT CCAGTTGACT TCAGCTGTTT CCATGCTCTG CCCTATCCCC CAACCTCACC 840 TCCTTGAGTG AACAATCCTC TCCCCTACTT GGTTCCTATT TGAATTGTTC TTCAGTTACT 900 GGCATGTATT TGAAATTGTA ATCACTCTTC ATTCTTTAAT GCTTCTTCCT TTTCTGAGCC 960 TTATTTTTTA TCATTTAAAG CTTCTGGTGG GGACATTCCT ATACTTACTA ACATAAAGGC 1020 CAGTACCTAC TTTAGAATTA TTTGAGGACA GTTTCAATTT TTCATTACTG GGAGGAAAGG 1080
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