Tag | Content |
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EnhancerAtlas ID | HS188-11186 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr6:91060320-91061350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:91060581-91060599 | TCTTCCTCCCTCCCTCCC | - | 6.36 | ZNF263 | MA0528.1 | chr6:91060569-91060590 | TCACTCTCTCTCTCTTCCTCC | - | 6.11 | ZNF263 | MA0528.1 | chr6:91060576-91060597 | CTCTCTCTTCCTCCCTCCCTC | - | 6.5 | ZNF263 | MA0528.1 | chr6:91060586-91060607 | CTCCCTCCCTCCCTCTCCTCT | - | 6.6 | ZNF263 | MA0528.1 | chr6:91060580-91060601 | CTCTTCCTCCCTCCCTCCCTC | - | 6.71 | ZNF263 | MA0528.1 | chr6:91060572-91060593 | CTCTCTCTCTCTTCCTCCCTC | - | 7.1 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_58370 | chr6:91058940-91135531 | Ly1 | SE_59753 | chr6:91059505-91108225 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 91060788 | 91061282 | chr6 | 91060521 | 91060684 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I090350 | chr6 | 91059902 | 91061387 |
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Enhancer Sequence | TCAATAAATA TTTGGGGAAT AAATGTATCT GTATTTGCTT GAAATGGACA AGTGATATGG 60 TTTGGCTCTG TGTCTCCAAC CAAATGTCAT GTTGAATTGT GATTCCCAGT GTTGGAAGAG 120 GGACCTGCTG GGAGGTGATT GGATCATGGG GGCAGATTTC CCCCTTGTTG TTCTTGTGAT 180 AGTGAGTGAG TTCTCATGAG ATCTGTTGGT TTAAACACGT GTGGCACTTC CCTCTTTGTG 240 CTCTCTCTCT CACTCTCTCT CTCTTCCTCC CTCCCTCCCT CTCCTCTGCC ACCAGATGAC 300 GACATACTTG CTTCCTCTTC ACCCTTCTGC CGTAATTGTA AGTTTTTTGA GGCCTCCCAA 360 CCATGCTTTA TGCTTTCTGT ACAGCCTGAG GAACTGTGAG TCAATTAAAC CTCTTTCCTT 420 CATAAATTAC CCAGCTCAGG TAGTTCTTTA TAGCAGTGTG AGAACAGACT AATACAACAA 480 GGTTCACGTA TTTTTCCTGT AAGGCCCCCA AAGTTCTGCA TACATCAGTG GATGCAAATA 540 GATGCTTTGA GGAGGAATAT CACCATCTCC AGCTGTCAGG CTGATCGAGT CTGATTGGCA 600 CCCACTAGGA TTTCCCTTAC ACATGTAACA TGTGGGCTGC TGGAGGCAAA GGTAATGTTT 660 AGTAGACCTC ATTCCTCATA TCAGATCCAA CCTTCCTTGT CATCTCTTCT GACTGTCTTT 720 CTGTTTCTGC TGGTTTGCTC AGAGCCTGTC ACTGCAGCAC CTAATCAGGC CGATCTCTTT 780 AGCACTGACC TAGTCTGGTG TTGGACTTCT CTCCTTGTTA TCAAAACATA CCTCCCTCTT 840 TCCTCAGTTC ATGAAGTTGG AAGACACTTC TCTGCTACTG TGTGGTGATG GGGGCGTTAG 900 TGGGGTAAAC AGTTTAACTG TTTTAACTTC ATTCGTGGTT AAGAGGTACC AGGGGCCCTC 960 TGATAATAAA ACACAGCTAA GATGTATCTA AGGCTTATAG AAAGCAACAA TAAACCATTT 1020 TTGACTGTGC 1030
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