| Tag | Content |
|---|
EnhancerAtlas ID | HS050-28495 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:36480100-36481490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr17:36480478-36480489 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr17:36480478-36480488 | GCCCCGCCCC | + | 6.02 | | SP3 | MA0746.2 | chr17:36480477-36480490 | CGCCCCGCCCCCC | + | 6.11 | | ZNF263 | MA0528.1 | chr17:36480980-36481001 | CCCCCCTCTCCCACCTCCCTT | - | 6.23 | | ZNF263 | MA0528.1 | chr17:36480977-36480998 | CTTCCCCCCTCTCCCACCTCC | - | 6.95 | | ZNF740 | MA0753.2 | chr17:36480481-36480494 | CCGCCCCCCCCAC | + | 7.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I038323 | chr17 | 36479702 | 36481743 |
|
Enhancer Sequence | ACTCCCCTGG ATATCTCAGG GTTCTCTAGA TAATCCTAAA TAGGAGCTAA GCAGTAGCTG 60
CCACCAGAGA GCCAGAGGAT GAGTGCAATT TCCATTTCCC CTTGGGATTA AATCCAGCTG 120
AGCAAATGGC CTCCAGATGT GAGGGGCTGG CTAGAAGGAC CAGGCAGAGA CCATCTGCAG 180
TGTCAGCACT GACCTGGGCA CTAGCAGAGC ATTAGCCAGA TAACCCAAAG TCCCAAGACT 240
GCAGTGCACC TTGAGCTTTG GAGCAGGCAT TGTTCTTTCC TTATCTATCT TCTGTTACTG 300
TTTAAAAATG TTAAAAAAAG ATAATCATGA ATAAGCTAGA GCCAACTGCA ATGTCAAGAA 360
AAAGCATTCT TTATTTCCGC CCCGCCCCCC CCACCCCATG GTTTATTTCA CAAGAGTGTG 420
TTTGGCGGCA ACTTTGCTGT TTCCAGCTAG ACCAGACCCA ATGGGATTGT TTTGGGGTGC 480
ACAGCAAAAT CCACTTTAGC TCAGAAGCTG TAAGGCTAAC TAGCCAGAGC CCAGAACAAC 540
AACACACTTC AATTACTGCT CCAAAAGCCC AGAATAAGGG CCCTAGGTAA GAGAATGAGG 600
ACATCTGGTC CCCAAAGGAG AGTAGGTTAC TCCATTCCTC TGTTCCCTTT TGGAAATGGA 660
GTACTTTTTT ACTTTCTCTG TGAAGTCCCA TAACCGCCCA GCATATTTAC ATGCAGACTA 720
GATGTTAATG GCTCTTTTTC CCTTTGGGTA TTTGGTCTCC CTGTTTGTCT TTTTCTCCCC 780
ATGAATGACA TCAATGTCTG TACTGTTGTA CTGTTAGAGG GCGTGACTTA CTGCCATCTT 840
TAGTGCCCCT GTGCAGCTCT GCCTTCTCTA GCTGCCCCTT CCCCCCTCTC CCACCTCCCT 900
TTGCCAATCT TGGGACTTCT TTGTATGTTT TTCTCCTTCT TCCTTTCCCT CTGGTATTAT 960
CATCTAATCC CAGCAATTTG TAATCTAGTA CTGCTTAAGC AAGTGTAGCC TGAACTGACG 1020
AGAGAAGGGA GCCAAGAAAG AGAGAGCTCC CTAAGAAAGA AGGCTTTGTC TTCACACAGT 1080
GCCCTTTTCC CAGCTCTCAG GCTTCTAACT TGCCCTGTAG CACTCCTCTT TTAGAGGGCA 1140
GAAGAAGTAG AGTGCTGGCT GTGTACAGGA CTGCCTTTCT TGAGCTCCTC TGGAAGGAGA 1200
TTGATGTGGC CTCTTGTTAC TGAGCAAGTG ATTCTTGGGC GGGGAGGGGT GGGGGAGGGT 1260
GGATGGGTCT TGCATCAGAA CCAGAGATTC CCCTTGACTC CAGTTGCCTT GACAAAAGAG 1320
AGAGGTCCTG TTGATGGCAG CGCTGAAAAG CTAGGGGGAA GGAAATGAGC CAGTGAGACG 1380
AGCTCTGGAG 1390
|
