| Tag | Content |
|---|
EnhancerAtlas ID | HS043-02831 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:160971140-160971840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:160971522-160971540 | GGAAGGAAGCCAGCAGGG | + | 6.43 | | Nkx3-2 | MA0122.3 | chr1:160971318-160971331 | TTTAAGTGCTTTT | - | 6.03 | | PHOX2A | MA0713.1 | chr1:160971414-160971425 | TAATCTAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr1:160971414-160971425 | TAATCTAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr1:160971414-160971425 | TAATCTAATTA | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27895 | chr1:160970135-160971772 | Fetal_Intestine | | SE_28868 | chr1:160970480-160971793 | Fetal_Intestine_Large |
|
| | 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 |
| GH01I161000 | chr1 | 160970136 | 160971793 |
|
Enhancer Sequence | AGCCTAAGGA GAAAGAAAGA GGTGGGCCCT GTCAGGAGTG GACAGAGAAA TGCCAGGAAG 60
AAGGAGTCAC AGACCCAGTG GACAGGGCTT CTCCATTCAC AGACCCTAAG AGGAAGGGAT 120
TCCAGACTTA TGCTCCCTCT GGCTCTCACA CTTTGTCACC ATGATCCTAA ATGTCTTCTT 180
TAAGTGCTTT TTGCTACAAT TGCCAGCTAA TACTTCTTTT ATCCATGGGA ATGCAGTTTC 240
TTTTGCTTCT AATTTTTCTC TCTGTGACTC CCAATAATCT AATTAGATTT CTACTAGTCC 300
AAGGGCAGCT TCCAGAATGA CATTTCACTG TTCAGAGAAA GCTTCTCAAC AAATGATTGC 360
AGCCACTTGT CAGGACAATC CTGGAAGGAA GCCAGCAGGG CTGGAGGCAA GGGATGGAAG 420
GGAAGGGCAG AGCCATGATG AGGATAATAA TAATACTCGA CATTTGTGGA GCATGTGGTG 480
CTTTTAAAAG TGTTTTCGTG TACATTATGA CACGTTGCAT CATTTGATCC TGGACACAAG 540
CATGACAGAT CGGCAAGACG TATATTATTA TCCCGAGTTT ACATGAGGAA CTGAGAGTAC 600
AAGAAGTAAA TGTGCCTAAG ATCACACAGC TGGGGCCAGG TGCGGTGGCT CAGGCCTGTA 660
AACCCAGCAC TTTGGGAGGC CGAGGTGGGG AGGTCATGAG 700
|
