| Tag | Content |
|---|
EnhancerAtlas ID | HS182-17872 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:139933010-139934490 |
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 | chr5:139933604-139933619 | 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 | AACATGTACT AGGTCGAGGT TAGAGCAGTG CCCAAGAAGC AGGAAAACTT TTGATTTGTT 60
CAAGAGACAG TAATGAGGCC TGTATGGCTA AAAATTATTA CCACTGAAGA AAGTAGTATG 120
AGCTATCATT AGAGAGGTAA GCAGAGGGTC CAGACCCTGT GGGGCTTTGG AAGAGTTTGA 180
TCTTGAGTCA ATGGTACTGG GAAGCCACTG CAGGTTTGTA AAAGCAAGGG GTGATGTGAC 240
CAGACTTATT TTTAAACATG TATGCTCTGT GAAAAACTGA TGAAAACAGG TCAACAGTGG 300
TGGCAGGAAC ACCAGTTGAG AGGTTGAGTA GTTCAGGAAA GAGATAATGC TGGCATGGAC 360
TAGGGTAAAA GAGTAGACGA GGGGAATGGA GTAGTCTGAG ATTTACTTAG GAGGAAGTAG 420
CAACAGGAGT GGATTGAGAG TGAGGAAGAG AGAAGTCAAG GTGACTCGTA GTTTCTGACT 480
TAGTAATGGG AACCACTAAC AGAAAGAAGA CTGGAAGACA AAAGTCAAAA GTTTACTTTT 540
AGGTACCAAC ATCCACAAGG ATGATTAATT CATCTAATAA TTTGGTGTTT CAGTTGACCT 600
CTTCACCTCC AGTGATCATT TTTTCCCACC CTACATCAGC CTGTCATCCC CCTGCCTTGT 660
TCACACTATC ACCTCCAAAA TCTGATCACC CCCTTACCCC TTCCAGCTCA GCTACTTTGA 720
TTTCAATGTA CATTAACATC ACCCCCTTAT AAATATTTTT ACCTCCTTTA TCTCCTCCCA 780
TTGTCCCACT TTCCTGGTTA AACCCAACTT GCTTGCACTT GGGAGGGAAA ACAGAGCCAT 840
GCTGATAGTT TAAATTCATG GCCACAGATT TTAAAAGGTA CCAAATACTG CCTGGACATT 900
TTGGCTCATT TTTTCCACTC TTCAGAACTT CTCTTCCTTT CCTTGCTATC TTCTTCTGAC 960
ACTGCCTAAT GTTTCATTGA AAAGTAGAGG TCATTAAACA GAACTCTCTC ATCTTCCCAC 1020
CACCATTCCT CCTAACCCAC CTGCATCTGT GGCCACTTTT CTTCCTCTTG TAATAGATGA 1080
AAAGGTTCCT GCTCCTATCA AAAGCCATCT TACCAGCTGT ACTCTGCATC CTAGCCTCTC 1140
TTGTCTTCTC TAGACTTCCC TACTGTAACT ATCTTCTCTT GCATCATCAG CTCCCCCTCT 1200
CTACTGAATC ATCCCGTTAG TGTACAAACA TGCTCTAGTA TATTACTATC AAAACACTCC 1260
CTTACTTCAT GTTCCATTTT CAGATACTGT CCCATTTCTT ATCTCTGCAG CAGCATTTGA 1320
GTGAGCTCTT TATAGTCACT CTCTCTACTT TTCACATTCT CTCCTCAGCC CATTCCAGCT 1380
GTTTCTGTTC TCACTACTGC AGAGACTTGC TCTTGTTATG ATCACGAGTG ACTGCTATGT 1440
TTGTCAAATC TACTGGTTCC TTGTCGCTCT TTTTTTTTTT 1480
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