| Tag | Content |
|---|
EnhancerAtlas ID | HS120-04954 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr4:113033700-113035180 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr4:113034722-113034733 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr4:113034722-113034733 | ACAGATAAGAA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 113033871 | 113034904 | | chr4 | 113034135 | 113034634 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I112112 | chr4 | 113033251 | 113035216 |
|
Enhancer Sequence | AAGATAAATG GACAATAGCA GGTGAGAAAT ATCTCAACAA ATTTAGTGGA AAAGAAGATG 60
GAGCAGAAGT AATTAATTTA GCAGTGTAAC CTCAGGGTCC ACAGAGGGAG AAACTAGTAA 120
AGCTAGCCAA TGTGTTATCT GGAGGCTTGG GGCTAGAACA GCAGAGTTCC TATGGGAAGT 180
AGGGGTGAGG CTCAAGCTGA AATCAGGGCC TAGTTGAAAG ACTGTACAGT CTGTTTGTTT 240
ATGAAGCAGC TGGAAGTCTA GGCCCCTTTC CCACTTCACC TCACCCATCA AGGACCAGAA 300
ATTCACTCAG AGAAACCCTG AACTCCTGAA ACCAAACATA GTGTGGCAGA TGGAAGACTG 360
AAAATAGGGG GTGGGGGATT AAGTGAAAAT CTGGATGCTG AAACTAAGAC TTTCAGCTGC 420
TTTTTCTACT CTACATTCAG AACAATAGCA GCCAGACTTA CACACCGACT CTGTCACATT 480
TGCCCCTCCA TCCCCAATTC ATATTTAAGT ACATTGAAAG GATTCTTGAG AAGCGTGTGA 540
CAGAGATATC ATAAGATCTG GAAAATCAGC AAGAAGATCT TAGCAAACTT GGCAAATGAA 600
AAGGGAGAAT TATTAACTGC AGGGAAAAGT ATTATATGAG AAAGAGGTGT GGTGTAGTGC 660
ACAACATGGC TAAACATTGC GTAACATTTG CACAGTCATG ATAATGTAAA CACTGAGTAT 720
TGGTTTAGCC AAAAATGCTA ATGTAACTAC ATCAGGGGAT AGGGGAAGGA AACTGATGGA 780
ACACAGGAGT TTTCTAGGTA TTATTGTTTG GCCTTCAACA TACATTCGCA CTCTTTCCAC 840
ATACCCCCTT AATTACAAAG GCTGGGAAGC TAAAAATGAC CACATTTCCC AAAAGGTCCT 900
GCAGCTACAG TTCTGGACAC AATTTAAGTT CTCTCATAAG ATGCACTCAT TTGAGATTTG 960
GAAGGCAGAA GTGAGGCAAA GGCCATTTTC TTGTGACTGA GGCAGCTGGT AAACAAGATT 1020
AGACAGATAA GAATGTTTGC AGTAGGCCAG GCACAGTGGC TCACGCCTGT AATCCCAGCA 1080
CTTTGAGAGG CTGAGGCAGA TGGATCACCT GAGCTCAGGA GTTTGAGACC AGCTTGTCTA 1140
ACTTGATGAA ACCCCGTCTC TACTACTAAA AATACAAAAT TAGCCAGTCA TGGTGGTAGG 1200
TGCCTGTAAT CCCATCTACT CAGGAGGCTG AAGCAGGAGA ATCGCTTGAA CCCAGGAGGT 1260
GGAGGTTGCA CTCCATTCTG GGTGGCAGAG CAAGATGCAG TCTTTAAAAA AAAAAAAGAA 1320
GAAGAAGAAG AAGAATGTTT GCAGTAGGCA GACTTCACAT CCTAATGTGT CTTCATGGAT 1380
GTGGGGCATT AGCAGAGGTG ACAACAGCAG CCACCTGACC TCTGTATCAA CCCTACTCTA 1440
CATGGTATGC CACTGAACCC AATAGTCCTG CAACAGCCTT 1480
|
