| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11241 | Organism | Homo sapiens | Tissue/cell | GM19238 | Coordinate | chr4:159642890-159644350 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr4:159642918-159642929 | TTCAAGGTCAA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTGAAATC CACCATTCCA TTCTCTACTT CAAGGTCAAC TTTTTAGAAA CCACATGTAA 60
GTGAGATCAT GCCTTGTCTT CCTGTGCCCA GCTTATTTCA TGTAACATAA TGTCCTCCAT 120
ATTAATTCAT GTTGTCAGAA GTGACAAGAT TTCATTATTT TTTATGGGTG AATAGTACTC 180
CACTGTGCAC ATATATCAAA TTTTAAAAAA AATCCATCTG TAGATGGAAA CCTAGTTTGA 240
TTCCATTATC TTGGCTATCA TGAATAATGC TGCAATGAAC ATGGGAGTGC AGATACCTCT 300
TTGACATACA AACTTCATTT CCTTTGAATA TACTCACTAG AATTAGTGAA TCTTATTTTA 360
TTCTAATATT CAAATTTAGT CTACCTACTG TCATGTATGT ATATAAACAG ATTTGAAACA 420
TTACACTAAG GATCATAACC AATTATAGTA GCCAAAAGAT TAGCACCATG TAAGAGATAT 480
CATTAAATAC AAATAGTTTT AAATCCTGAG TAATTTCTTC AAGAGGTACT GAGAATTTCC 540
AATCACCAAG CAACCAACGG GAGAAAATTA AACAGTCTTT GGGTGGGCGG ACTTGCCACG 600
TGTTACGTAT ACCTGCAGCC TTTGTGCTCT GAGCAAACTG CCTCATGCAA CCTCTGAAGC 660
AAAAGCTGTA AAAATTCCTC CTCTAGATAG CAGCTAAGAC AGGTGAGATT AAACCTAGCC 720
CTAGCTAGTT GCAACAAACT GAATGTACGT GTAAACGTGT GTGTGTCCTG TACATGCATT 780
CAAACACATT GCCTGGCCAG CAATTCCAAC GTGTTCCAGA ACAAGGCCAA TCCAGTTACA 840
AAGCAACACG CTCCCTAATT CACCAGGCCT TAGGAACTTC TGAGCGGCTA TGTAACCTAG 900
GCAACACCAT CACTACGTTG AGCGCATTTT CCCAATGGCA AATTAAGAGA AAATGTTTGC 960
TCATCTGAAC GGACCTCTAA ATTAAGAATC AGTAATAAGG CAAAAGCAAT GAGCAAACAA 1020
GTCCCTTTAA CGTATAAATA ACACAGCACG TGCTGATATA TTATCTCATG TGGCAAATAT 1080
AGTTTCCTGG GGCCCAGCAG ACGCATATCC CAGGATATGC TTTCCGAACT GTCCCATTGC 1140
AAACATAAAA TATTTCATGC TAACTTGGTA GTGCAAAGGT GGCGTGGAAG TGCCACCAAA 1200
TCAGGAGGCA AACCTAAAGG ACGCCACAAT TCCCGAACTA GAAATTTCCA GAAACTTCCG 1260
CACCACCGAT GGCATTGATA CAAGGGCGCT GGATCGATCT AGCCCTAGAT CTCCGGGCCT 1320
GCTCCGGCGG ACCAGCCTAG GCAGCCATCC CCTCCGCGAA ACTGAGCAGT CACCGGCCGG 1380
AGCCGCATTC CGCCCTTGGA ATCCCCCAAA TCCCGGGAAC CCCCGCCTCC TCGGGGCTTT 1440
TCCGCGAGCG TCAGACTCCG 1460
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