| Tag | Content |
|---|
EnhancerAtlas ID | HS104-40494 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr3:48918020-48920290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr3:48919319-48919331 | GCTATTTATAGA | - | 6.37 | | MEF2B | MA0660.1 | chr3:48919319-48919331 | GCTATTTATAGA | - | 6.27 | | RREB1 | MA0073.1 | chr3:48919281-48919301 | CTCCAAAACAACCCCATCCA | + | 6.68 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTTTTTTG AAACAGGGTC TTGCTCTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCTC 60
AGCTCACTGC AACCTCCATC TCCTGGGCTC AAGTGACCTT CCCACCTCAA CCTCCTGAGT 120
AGCTGGGACT ACAGGCAAGC CGGGCTAATT TTTGCATTTT TGTAGAGACA GAGTTTCGCC 180
ATGTTGCCCA GGTTGGTCTC AAACTCCTGG GCTCAAGTGA TCCTCCTGCC TTGGCCTCCC 240
AAAGTGCTGG AATTACAGGT GTGAGCCACT GTGCCTGGCT ACCTCCTTTT CTTTCTGGGA 300
TTAGCAATAC CAGCACGGTT TGGAGGCAAT GGGGCACAAA GTTACATTTA GCATTTCAAC 360
AGAGTTCCAC AACTTAGCAA ATGTTACTGA AAAACTTCAC CTACTGTCCT AAGCTTCGGT 420
GCACTCTTGA CCCCAAGCCT CCAACAACTG AGCCTTCAGG TCAGTCCCAT CCAACAAGGA 480
GCTTATGAAC AGATGCCAAA TGGGGCTAGA GGGACATCCA CTGTAAAGAG TTCACTCCAG 540
GCAGGGCACC AGTTTCAACA GCGCGATTTC TCCCTGCATT CACCCCAGGC AGGGCTCATG 600
CATCTACCTC AGGCACACAG CCAAGCTGAC TGTCAAACAG TCAAGAGACT TGCTTTCCAA 660
CACGGCCATC TTCACAGTCC CAGTTCACAT GGCTATCCCT GAGGAGTCCT CTCAGCAACT 720
AAATTCTCCC TATGAGACCA ACATGTTCCA TTTTCCCCAT AATGCCCAAC CCTAGGCTCA 780
GCAAACCTCA TCTCTTGGGA CTGGAGACTG TCTCTGAATA GGATCTCTGT GTGTGCACAG 840
GGTGTCATGT GGACACTCAA TGGCTGCCTG GCCTATTCTC CCACTCCCCA CCCCCATCTC 900
CATCCCAGGG AGGCATCTTT GAGAGCTAGA CTCTCCTGGA CTTCCACCCC AAGGCCCTGG 960
TAACACTCCT TTCCATATCA CCCCCAAACA CCATTCCAGG GAGGTGAACA CAGCAGGGCT 1020
GACAGGATTG TGGGAGTGGG GTCCTGAGTG TCTTAACTTT GTTCAGTCAG GAAGACTGTT 1080
TTTCTGAGTG CTGATGTGAC TGTACAGGAA CACAGCCCAT AGTCCAAAGT ACCAGAAGTG 1140
ACCCCACGGG GGTCATGCAT GGCCCTGATA CATCCGTGAG CTGGCACACA TGCTAAAAGA 1200
CCAGGCGCTC AAAGAGGGCA TGTGTCTGTG GGACACAAGG ACTATCAATG GGCAAATGCA 1260
GCTCCAAAAC AACCCCATCC ACATTTCAGG ACACTTGCAG CTATTTATAG AATCTAGGGA 1320
CATTCAGAGA GTCATAAGGA TCCCAGAAAT AGAGTTTCAC TCTACAAGCA CCTCCATCTA 1380
CATCCTAGAC CCTCACTCAG CCTGCTGTGG CCTGAAGTGG TGACAGAATA CAACCGCATG 1440
GCGCCCTGGG CTTCCTCCCT TGAGCTCCTG GATCTGAGGG CAGGCCAGCC TCTGTGGCTC 1500
CTGTACTGCC TATAGCCCCT CCCAGGGGCT GGCATCCTGC ACAGCTCAGA TTGTGGATAC 1560
CTTTTCACCC AATATTTCCA CTCAGAATTT CCCTGCCTCC TGAGAAGCCT CTGTTTTCAT 1620
TAACTACTTT GTAAATTCTG AACTATAATT CTGTCTCAGG TGACTCTTCA TACCCAAATC 1680
CAACTTCTTA AAGTTTATTA AAGGAAAACA CATTAACTTA TTCCACTTTA ACAGAGAAAC 1740
TAATACCTGA AATCTTTATA GTCATATTAG CATGCTGTAA AAATGAAGCA CAACAAAAGT 1800
TGGAACCTTC TCTTCTCTCA ATCAGGTGAT AGAAAGCAAG GCTGTTCTTG TCTTTAGGGC 1860
AGCACCAGGT GCTGCCTATG ACATGTCACA TATATTTAAG CATTCAGACC TCTCAACAGC 1920
CTCCTGGGGT TGGTATTACA AATCTCTCCA GTAATTGATA CTACCTTATA AAAGAAATAC 1980
GAAAAACTGG TCAGGTGTGG TGGCTTACAC CTGTAATCCT AGCACTGTGG GAGGCCAAGG 2040
CAAGAGAATT GCTTGGCTCC AGGAGTTCAA GACCAGCCTG GGCAAGATAA TGAGAGCACC 2100
CCCCGCCGCC CCGACACACA CACACCGACC ATTGCTAAAA AAAATTTAAA AATTAGCCCA 2160
GAGTGATGGT GTGTGCCTGT AGTCCCAGCT ACTTGGGGGG CTGAGGCAGA AGAATCACTT 2220
GAGCCCAGGA GTTCAAGGTT ACAGTGAGTC GTGATTGCAC CACTGCATTC 2270
|
| |
|
|
|
