| Tag | Content |
|---|
EnhancerAtlas ID | HS187-20102 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:139933040-139935020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr5:139934305-139934316 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr5:139934305-139934316 | TTCTTATCTCT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr5:139934682-139934697 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr5:139933604-139933619 | TGACCTCTTCACCTC | - | 6.67 | | RARA | MA0729.1 | chr5:139933601-139933619 | AGTTGACCTCTTCACCTC | - | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr5 | 139933633 | 139933898 | | chr5 | 139934000 | 139934200 | | chr5 | 139933602 | 139933696 | | chr5 | 139933966 | 139934426 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I140553 | chr5 | 139933159 | 139934863 |
|
Enhancer Sequence | CCCAAGAAGC AGGAAAACTT TTGATTTGTT CAAGAGACAG TAATGAGGCC TGTATGGCTA 60
AAAATTATTA CCACTGAAGA AAGTAGTATG AGCTATCATT AGAGAGGTAA GCAGAGGGTC 120
CAGACCCTGT GGGGCTTTGG AAGAGTTTGA TCTTGAGTCA ATGGTACTGG GAAGCCACTG 180
CAGGTTTGTA AAAGCAAGGG GTGATGTGAC CAGACTTATT TTTAAACATG TATGCTCTGT 240
GAAAAACTGA TGAAAACAGG TCAACAGTGG TGGCAGGAAC ACCAGTTGAG AGGTTGAGTA 300
GTTCAGGAAA GAGATAATGC TGGCATGGAC TAGGGTAAAA GAGTAGACGA GGGGAATGGA 360
GTAGTCTGAG ATTTACTTAG GAGGAAGTAG CAACAGGAGT GGATTGAGAG TGAGGAAGAG 420
AGAAGTCAAG GTGACTCGTA GTTTCTGACT TAGTAATGGG AACCACTAAC AGAAAGAAGA 480
CTGGAAGACA AAAGTCAAAA GTTTACTTTT AGGTACCAAC ATCCACAAGG ATGATTAATT 540
CATCTAATAA TTTGGTGTTT CAGTTGACCT CTTCACCTCC AGTGATCATT TTTTCCCACC 600
CTACATCAGC CTGTCATCCC CCTGCCTTGT TCACACTATC ACCTCCAAAA TCTGATCACC 660
CCCTTACCCC TTCCAGCTCA GCTACTTTGA TTTCAATGTA CATTAACATC ACCCCCTTAT 720
AAATATTTTT ACCTCCTTTA TCTCCTCCCA TTGTCCCACT TTCCTGGTTA AACCCAACTT 780
GCTTGCACTT GGGAGGGAAA ACAGAGCCAT GCTGATAGTT TAAATTCATG GCCACAGATT 840
TTAAAAGGTA CCAAATACTG CCTGGACATT TTGGCTCATT TTTTCCACTC TTCAGAACTT 900
CTCTTCCTTT CCTTGCTATC TTCTTCTGAC ACTGCCTAAT GTTTCATTGA AAAGTAGAGG 960
TCATTAAACA GAACTCTCTC ATCTTCCCAC CACCATTCCT CCTAACCCAC CTGCATCTGT 1020
GGCCACTTTT CTTCCTCTTG TAATAGATGA AAAGGTTCCT GCTCCTATCA AAAGCCATCT 1080
TACCAGCTGT ACTCTGCATC CTAGCCTCTC TTGTCTTCTC TAGACTTCCC TACTGTAACT 1140
ATCTTCTCTT GCATCATCAG CTCCCCCTCT CTACTGAATC ATCCCGTTAG TGTACAAACA 1200
TGCTCTAGTA TATTACTATC AAAACACTCC CTTACTTCAT GTTCCATTTT CAGATACTGT 1260
CCCATTTCTT ATCTCTGCAG CAGCATTTGA GTGAGCTCTT TATAGTCACT CTCTCTACTT 1320
TTCACATTCT CTCCTCAGCC CATTCCAGCT GTTTCTGTTC TCACTACTGC AGAGACTTGC 1380
TCTTGTTATG ATCACGAGTG ACTGCTATGT TTGTCAAATC TACTGGTTCC TTGTCGCTCT 1440
TTTTTTTTTT ATTGAGATGG AGTCCCAGGC TGGAGTGCAA TGGTGCGATC TCGGCTCACT 1500
GCAGGCTCCA CCTCCCAGGT TCAAATGATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA 1560
TTTCAGGTGC CCGCCACTAC ACCTGGCTAT TTTTTGTATT TTTAGTAGAG ACAGGGTTTT 1620
ACCACGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCGTG ATCCACCCGC CTTGGCCTCC 1680
AAAGTGCTGG AATTACAGGC GTGAGCCACT GCGCCTGGCC CCTTGTCTCT ATCTTGATGT 1740
CTCAGCAGCA TTCATTACTA TTGATTCATG TCTTTACGCT CTCCTATTTT CTTTTTTTAT 1800
TTTGGTTTTG TCACAGAATA TCACTCTGTC GCCCAGGCTG GAGTGCAGTG GTGCGATGTC 1860
GGCTCACTGC AACCTCCGCC TCCCAGGTTC AAGCGATTCT CCTGTCTCAC CCTCCCAAGT 1920
AGCTGGTATT ACAGGCCCAG CTAATTTTTG TATTTTTAGT AGAGACAGCG TTTCGCCATG 1980
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