| Tag | Content |
|---|
EnhancerAtlas ID | HS127-00306 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr1:19842710-19844200 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr1:19843976-19843987 | TTGACCTTGAA | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTTAGTAC AGATGGGGTT TTACCATGTT GGCCAGGCTG GTCTCAAACT CCTGGCCTCA 60
AGTGATCCAC CTGCCTCGGC TTCCCAAAGT GTTGAGAATG CAGATATGAG CCACTGTGCC 120
CAGCCTTAAG AAAAGAGGTT TAATTGGTTC ATGGTTCCAC AGGCTGACCA GGAACCATGG 180
CTGGGGAGGC CTCAGGAAGG TGAGGGAAAG CAGGCAAGTC TTACATGGCT GGAGTAGGAG 240
GAAGAGGGCA AAGCAGGAAG TGCTACACAC CTTTTAAACA ACCAAATCTC ATAAGAACTC 300
GCTCACTATC ACAAGAACAA CAAGGGGGAA CTTCGCCCCC AGGATCCACT CACCCTCCCA 360
CCAGGCCCCT CCTCCAACAC TGGGGATTAC AATTCCACAT GAGATTTGGG TGGGGACACA 420
AATCCAAACC ATATCAGGTG GGCTCTCACT ATGTTGCCCA GGCTGGTCTT GAACTCTTGG 480
GCTCAAACAA TCCTCTCACC TCAGCCTCCC AACATGCTGG GATTACAGCC ACTGCATCCA 540
GTCAACTAAG GAGCTTCTAA TTCCTCACCC TAGAGTTAAG CAGACTTAGC CACCCTGTTT 600
GAGTGCTTGG TGCTTTACTA CCCAGCACTG AAGTGAGCAG ACCTATGCTT CAGAGGTAGA 660
GCCTGGCCCT GTAGGACTTA AGGCATGGAG GAACAGAAGA GAAGGTGTGT TGGCAAAAAG 720
AACAGAAAGA AGGAACTCAG TGGAGCATGC CCAGTTCCTT CTCCCACACC CACCAGAGTG 780
TTATTCTTCC TCCCATGGGA AACAGTAAGG GAGGGGACCA AGAGCAGCTA ATATGTTACT 840
CTGATGGACC TCCTGCCACA TGGAAACTTG AAGCCAGAGC AAAGGAAGTT TGCCACCAAT 900
AGACACCTTG ATGAAGAATG AAGCAAAGGA GAGGCCTGGC CAAGGAACCC AGACACAGCT 960
TCTTGGCAAA GAAGATGACA ACTGCTTGAA TCAGAAAGCA GAACTAGGCT GGGTGTGGTG 1020
GCTCACATCT GTAATCCCAA CATGTTGGGA GGCCAAGGGA TTGCTTGAGG CCAATAATTA 1080
AACATCAGCC TGGGCAGCAT AGCAAGACCT CATCTCTACA AAAAATAAAA ATATAGCTAG 1140
GTGTGGTAGT GCACAGCTGT AGTCCTATCT ACTTGGGAGG CTGAGGTGGG AGGAGTGCTT 1200
GAGCCCAGGA GGTCAAGGCT GTAGAGTGAG CTATCATTAT ACCACTACAC TCTACCCAAG 1260
AAGAACTTGA CCTTGAAAAG GAAGTTTGCC TTCAGGAATA GTTCCAATAC TGGTAATACT 1320
TAGACCCTGT ATTAGTCAGT TCTCACACTG CTAATAAAGA CATACCCAAG GCTGGGTAAT 1380
TTATAAAGGA AAGAGGTTTA ATTGACTCAC AGTTCCACAT GGCTGAGGAG GCCTCACAAT 1440
CATAGCAGAA GAGCAAGGGA CGTCTTACAT GGTGGTAGGC AAGAGAGAGA 1490
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