| Tag | Content |
|---|
EnhancerAtlas ID | HS136-00187 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr1:19842680-19844440 | 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 | GCGCACTGCC ACACCTGGCT AATCTTTGTA TTTTTAGTAC AGATGGGGTT TTACCATGTT 60
GGCCAGGCTG GTCTCAAACT CCTGGCCTCA AGTGATCCAC CTGCCTCGGC TTCCCAAAGT 120
GTTGAGAATG CAGATATGAG CCACTGTGCC CAGCCTTAAG AAAAGAGGTT TAATTGGTTC 180
ATGGTTCCAC AGGCTGACCA GGAACCATGG CTGGGGAGGC CTCAGGAAGG TGAGGGAAAG 240
CAGGCAAGTC TTACATGGCT GGAGTAGGAG GAAGAGGGCA AAGCAGGAAG TGCTACACAC 300
CTTTTAAACA ACCAAATCTC ATAAGAACTC GCTCACTATC ACAAGAACAA CAAGGGGGAA 360
CTTCGCCCCC AGGATCCACT CACCCTCCCA CCAGGCCCCT CCTCCAACAC TGGGGATTAC 420
AATTCCACAT GAGATTTGGG TGGGGACACA AATCCAAACC ATATCAGGTG GGCTCTCACT 480
ATGTTGCCCA GGCTGGTCTT GAACTCTTGG GCTCAAACAA TCCTCTCACC TCAGCCTCCC 540
AACATGCTGG GATTACAGCC ACTGCATCCA GTCAACTAAG GAGCTTCTAA TTCCTCACCC 600
TAGAGTTAAG CAGACTTAGC CACCCTGTTT GAGTGCTTGG TGCTTTACTA CCCAGCACTG 660
AAGTGAGCAG ACCTATGCTT CAGAGGTAGA GCCTGGCCCT GTAGGACTTA AGGCATGGAG 720
GAACAGAAGA GAAGGTGTGT TGGCAAAAAG AACAGAAAGA AGGAACTCAG TGGAGCATGC 780
CCAGTTCCTT CTCCCACACC CACCAGAGTG TTATTCTTCC TCCCATGGGA AACAGTAAGG 840
GAGGGGACCA AGAGCAGCTA ATATGTTACT CTGATGGACC TCCTGCCACA TGGAAACTTG 900
AAGCCAGAGC AAAGGAAGTT TGCCACCAAT AGACACCTTG ATGAAGAATG AAGCAAAGGA 960
GAGGCCTGGC CAAGGAACCC AGACACAGCT TCTTGGCAAA GAAGATGACA ACTGCTTGAA 1020
TCAGAAAGCA GAACTAGGCT GGGTGTGGTG GCTCACATCT GTAATCCCAA CATGTTGGGA 1080
GGCCAAGGGA TTGCTTGAGG CCAATAATTA AACATCAGCC TGGGCAGCAT AGCAAGACCT 1140
CATCTCTACA AAAAATAAAA ATATAGCTAG GTGTGGTAGT GCACAGCTGT AGTCCTATCT 1200
ACTTGGGAGG CTGAGGTGGG AGGAGTGCTT GAGCCCAGGA GGTCAAGGCT GTAGAGTGAG 1260
CTATCATTAT ACCACTACAC TCTACCCAAG AAGAACTTGA CCTTGAAAAG GAAGTTTGCC 1320
TTCAGGAATA GTTCCAATAC TGGTAATACT TAGACCCTGT ATTAGTCAGT TCTCACACTG 1380
CTAATAAAGA CATACCCAAG GCTGGGTAAT TTATAAAGGA AAGAGGTTTA ATTGACTCAC 1440
AGTTCCACAT GGCTGAGGAG GCCTCACAAT CATAGCAGAA GAGCAAGGGA CGTCTTACAT 1500
GGTGGTAGGC AAGAGAGAGA ACTTGTGCAG GGAAACTTCC CTTTATAAAA CTATCAGATC 1560
TCGTGAGACT TATTCACTAT CATGAGAACA GCACAGGAAA GACCTGTCCC ATCATTCAAT 1620
TACCTCCCAC CACGTCCTTC CCAAGACACA TGGAAATTGT GGGAGCTACA ATTCAAGATG 1680
ACGTTTGGGT GGGGACACAG CCAAACCATA TCAGACCCCT TTATAGGTAG GAAGACAGAC 1740
TCTGAGAGTA TTGCCTCCAG 1760
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