Tag | Content |
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EnhancerAtlas ID | HS188-09641 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr4:6989290-6990490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr4:6990150-6990161 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr4:6990149-6990160 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr4:6990150-6990160 | TCAAGGTCAT | + | 6.02 | IRF8 | MA0652.1 | chr4:6989954-6989968 | ACTTTCAGTTTCGT | - | 6.79 | IRF9 | MA0653.1 | chr4:6989954-6989969 | ACTTTCAGTTTCGTG | - | 6.25 | Nr5a2 | MA0505.1 | chr4:6990146-6990161 | GAGCTCAAGGTCATT | + | 6.51 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27343 | chr4:6987640-6990525 | Esophagus | SE_27664 | chr4:6986645-6990188 | Fetal_Intestine | SE_28549 | chr4:6986220-6990418 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGTACTCTTT GTGTCTGTGT TTCCACGTAT TTTCTTCTGG TTCACGTTTA CTAGGACGAC 60 GAGAGACAGC GTGAGCGAGC ACGTCCTTTG AGTCCTCCTT ACCCTGTTTT CAGAGCCGGG 120 CCAGGCCCAG CAGCCCCCTT AGAGGTCAGA AGGGCCTCGC CTGCGATCCG ATGAGCCTTT 180 GTATGGAGAT GAGACTGCGC TCCGAGCTCT AGAGCCCAAT GAGGTGGTCA GGTTGCAACA 240 GCAACCGGGC GTGTTAAAAC CTAGTTCCTT TGAATATGTT TCATTCACCA GCCCGCATAT 300 TAACTTTTGA TGCTCTGGGA GGAATATGAC TATTAGAAAA GGACTCCTGA GAGTGCTTCC 360 CAGAATGCCA ACATTCCCAG TAACTTAGAG AACGCTTTCC AGGAGGGGAC TGCAGCTTGT 420 TAAAGAACCC AGGCCAGAGG AACCACTCAG ATGTTCTCAG TGGCTTTACT TACTGTGAGG 480 TCAGGCTTCA GGGGTTAGCC GGGGCTGCCT TTTGGAAGGT GGGACCTTTC TAAGACCTGT 540 GCAGGCCATT CTTCCCCCTC AAAATGGCAA AACAGCCCCT CCCAGATGCT AAACTGGGCT 600 CCCCCCTCCA AGACAATTGC TTTTACAAAT GGCCAAGTGT GAGACCAGCC GCGGTGTTGC 660 GGACACTTTC AGTTTCGTGC CCTTTTCCAC AAGCAACCCT CTTAGAGTGG AATGTTGTGA 720 AGAGTAATTT CATAGTATAT AGTGACAGTC ATACTCCTAT CATTTCTGGG CACCTGCTTT 780 GGCTCTGCAG CTTATGCTGG TTCTCATTTA ATCTTCAAGT GTAACAGATG AGGAAACAGG 840 CTTGTGGATG GAGGAGGAGC TCAAGGTCAT TCTGCTGGTG GTGCTGGCTC AGACCAGGCC 900 TGCCGCTGTC CCCCAGCGCT TCCCTGGGTC CTCAGCCTGT GCAGATGTGG TGGCCGTGCT 960 GTCACAGCAT TAGTTCAAGT CAGTCTTTTG ATAGGTACCA CTCGGATGGC CAGCCTGCCT 1020 TGGCAGCTTT ATTCCAGGCG CGCTCCCAAA TCCTCAGGTT ATTTTCACTG GTGAATCTTG 1080 ATACTGCAGA CAGCGGGGTC GGAGATTTAA GCACAGGATT TGACTGATGA CCCTTTCCTC 1140 TTCTAGGTAA AATAGATTTC CAGGGAGCCA GAGGCTCCTT CCTGGAAGTC AGGGGGCTTC 1200
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