Tag | Content |
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EnhancerAtlas ID | HS176-29175 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:77658940-77659910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr4:77659266-77659284 | CTCTCCTTCCCTCTTTCC | - | 6.44 | MYCN | MA0104.4 | chr4:77659647-77659659 | GGCCACGTGGCT | + | 6.37 | MYCN | MA0104.4 | chr4:77659647-77659659 | GGCCACGTGGCT | - | 6.37 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02127 | chr4:77659023-77663265 | Aorta | SE_25862 | chr4:77656993-77661801 | Duodenum_Smooth_Muscle | SE_37143 | chr4:77658777-77660361 | HSMMtube | SE_38925 | chr4:77657891-77661587 | IMR90 | SE_44531 | chr4:77657722-77661457 | NHDF-Ad | SE_45238 | chr4:77657061-77661163 | NHLF | SE_45878 | chr4:77656953-77660920 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 77659496 | 77659694 | chr4 | 77659707 | 77659808 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I076735 | chr4 | 77657138 | 77661659 |
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Enhancer Sequence | TCTGTATATC TTCTTAGGAT TGGCCAGTTT TTAAATCAGG TTGTTTTCTT ATTGTTGAGT 60 TTTAAGTGAT TTTTTAAAAA CACATATATT TTGAGTTTCT AAGTAATTTT ATTTTGAGAC 120 AGCTTTCTGG AGTTTACAGT GATTGATAGT CTTTTTCCTC TTCTCCAGAC GGGCTCTGAA 180 AACCATCTGG AGGAGCTTGT AAATGAGAAA ATCTTGCCCT CCTAAATGTA TGAGGAGGCT 240 TTGCTTTGGC TTTTGGAAGT CATCCACAGG TGTTGGAATC CCAGCACCGA AGAGCCCCTG 300 TGATTAAGCC TTCTCATAAA GCTTCCCTCT CCTTCCCTCT TTCCCCTTAG TTCTGCCTCT 360 CATGAGCTTT TTCTGACTCT AATTTCTCTC ATTCAGCTTT GTGTTTAGCT TTCCCACCAC 420 AAACAAATTG TTTCTAGTGC AGTTAAGATT CCAGGAAGAT TGCCAGGGTG TATCCTTCAA 480 TTCCATAAAA AGGAAAGATA TTAACTAAAA ACATATACAT GTGCACACAA AGTCTCCTTC 540 ACCCGTGCCT ATTCTCTTAT TAACTTTTTC CCCTCTTCCC ACAAACAGCC CCAGTAGACA 600 CACAGTTTCA GTCTCAATCA CTCTTCTACC TCTCTCATTT CTTGGCACAT GCAAAATGTC 660 ATTTCCAGCA TGCAGCAAAT CACATCAAAG TGCTGCCTGT GCCCAAAGGC CACGTGGCTT 720 CCTCTGAGCT CCTCATTCCT CTCCTTGCTA GCCTGGGTGA TTAATTAGAG GCAGATAGGT 780 TAGAGTGTTG GGCAGTTACT CCTAGCGATG ACACAGAAGG AGGCTGAGCA AGGCCCAAAT 840 ATGGCCCTTT TTACCCACCC TTCCAAACAC CAAACCTCTT GCACAAGAGA ACATTTATAA 900 GCTGGGTCCT CTGCCTGTAA GCCTACTAAA TGATAACAGC TCAGTGGTAC TGACTGCTTT 960 GTCTTTCTTC 970
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