| Tag | Content |
|---|
EnhancerAtlas ID | HS121-01162 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr1:33413970-33415160 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:33414719-33414734 | GGTTAATCATTAATC | - | 7.52 | | HNF1B | MA0153.2 | chr1:33414720-33414733 | GTTAATCATTAAT | - | 6.05 | | HNF1B | MA0153.2 | chr1:33414720-33414733 | GTTAATCATTAAT | + | 7.22 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23323 | chr1:33413513-33414622 | Colon_Crypt_1 | | SE_23323 | chr1:33415006-33415566 | Colon_Crypt_1 | | SE_32111 | chr1:33414960-33415792 | Gastric | | SE_35956 | chr1:33413557-33414943 | HMEC | | SE_64575 | chr1:33414947-33415738 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 33414514 | 33414845 | | chr1 | 33414324 | 33414964 | | chr1 | 33414000 | 33414265 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I032945 | chr1 | 33411595 | 33415634 |
|
Enhancer Sequence | TGAGTGGGGG AAGAATGGGT AGAAAAAATA CCCCTAGTTA AATCCAGTTT GATTTAATTG 60
TTCCTAGGAG TATATATAAG AAATGAGGCA GCAGTCAAGA ACTCTTCACT GAACACTCCA 120
AATTGTACAA CCCACTTTAC TGGAAGGTTG GCTATGTCTA GACCTCAGGA ATTTTCATAA 180
AATGAATCCT GTCTCTTATT GAGCTGCCTA TCCCAACAAC TGGCATCTTA CACAGCACTT 240
GAACCACATT CTAGCAAGGA GATTTCCTTA GGGAGAAAGA TGTTTCCAAG AAAAATGAAA 300
TTTCTACCAG TCGATAGGCT GGTAGATTTA AAAGAAGAAT CCTACAGAAA GAATAGCCTG 360
CAGCCTGGAA TTAGCTTTAC ATTTTTAAAA ACTTTAGTTT GGGAAATTTA TTTTTCAGGT 420
TCAACATGTA TCATTGTGAT TTGCTGTTAA CATAGCCCAC AATCCCTTCC CATGATACTT 480
TCAAATTCAA AACCTAAAAA CAACTGGGTA TGCTATCTAC CATATACTTG GTAATTTTCA 540
GAGCAAGTTA TGAACTATCC TAATAAAATG ACAATTTAGG AAATTATGCT GTGCCAGGAA 600
AAAGTGAATG GCAAAATCTT TCCTACTAGC CTCTCCCAAA TGACATCAGC AAAATAAAAG 660
TACAAAGCAA TAAATCCACT GACATTTTAA AATAGGTTTC CTCTGACTCG CCAAGGTTGG 720
AGCTGAATGT GTGACATTCC TCCTTTTAAG GTTAATCATT AATCTATACT AATACTGTTT 780
CCTTTTCTTC AATCTGTACT CTACTTCCAA AGGCAGTGAG GCACTTAAGT CAGCTTGAAG 840
GCAAACAGCA CAGGTTTAAT ACTAATTAAA TGTCTTTCTG TTCACAATGA AAGTTTTGAA 900
AAAGCCCCTA GCAAAACAAA ATGAACTAAT TGCTCTCCAA TCTGAGACAT ATTACTAAGA 960
AAGTAGGAAC TACATAATTC AATTTTGTTG CATTTCAATT TTATATAGTT GGATAACCTA 1020
TAATGGTCAG AGAGGGAAGT GCTATCTTTA TTATAATATT GAAAGTATTA TCAAATGATA 1080
TTTTCTGCTC TCTGATCCTT TGGAGTACTT GGGTTATACA ATAAGATAAT TTCTTTCAGC 1140
TATGGGCTCA CATCATGAAA TACCAAATAA AGAGACAATG AGATAATGCC 1190
|
