| Tag | Content |
|---|
EnhancerAtlas ID | HS145-18617 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:183088290-183089250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr3:183088753-183088770 | AAGTACACTCTGTACTC | + | 6.15 | | Ar | MA0007.3 | chr3:183088753-183088770 | AAGTACACTCTGTACTC | - | 6.52 | | NFAT5 | MA0606.1 | chr3:183088943-183088953 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr3:183088943-183088953 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr3:183088943-183088953 | ATTTTCCATT | + | 6.02 | | NR3C1 | MA0113.3 | chr3:183088753-183088770 | AAGTACACTCTGTACTC | + | 6.08 | | NR3C1 | MA0113.3 | chr3:183088753-183088770 | AAGTACACTCTGTACTC | - | 6.18 | | NR3C2 | MA0727.1 | chr3:183088753-183088770 | AAGTACACTCTGTACTC | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 183088664 | 183088916 | | chr3 | 183089068 | 183089238 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I183369 | chr3 | 183086837 | 183090523 |
|
Enhancer Sequence | TGAATTTCTG AAGCAATCTA AATTGAAATG TCGAAAGATG GAACGTGGGT TTCTATCTGA 60
ACAAAACAGA ATAGATGACG CAAAGGCAGA ACAGTGAGGA GGTATTCTAA AACAATCACC 120
CAGGCAAATG AACAAAGAAA AGCCATCATA CACATATGAG GTCATTCCAC TGGGAAGAAG 180
TAACATCAGA CCCCTAGTTT TTAAATAGAG AAGGACAAGA GCCTGGCATA TTAACTTTGT 240
TTCCTGCCCT TTACTACAAT TTACTTAAAT TCTCGTGACA TGTAAGACTT ACTTGCCAGT 300
GCCACCATTT ACTCTTAATA AAACCAAGGA GTGCCTTCTG ATTTCAGGCC TCAGTTGGGT 360
GCCCAAAATC TAGCCTCTCT GGTATCCTCC CTGAGGGCTC TGAAGCAAAT CTACCCTCCT 420
TGGGCAACAC AGCTGCCCAC ATGACTGTAC ACTCTGGATT GACAAGTACA CTCTGTACTC 480
GTGACTGTAC ACTCTGGATG TACATCCTGA TGAGTCAGAT GAATGAATTC ATCTCCCTGA 540
CCCTTTGAGT CACAGTTCCA CAGCCAGTCC AGCGAAAACC ACACCTCACC CCAGCTACTC 600
CATCAAAGCA GCACTTTTGC TCGTTAATGT TGTTTAGACA CTTGAAAAAC AGTATTTTCC 660
ATTGCCTTCT GTGAACCCAA AAGTATCTGA GACAGGTCTC AATCAGTTTA GAAAGTTTAT 720
TTTGCCATGG GTAAGGTCGC ACCTGTGACA CAGCCTCAGG AGGTCTTGAC AACAAGTGCC 780
CAAGGTGCTG GAGGCACAGC TTGCTCTTAT ACATTTTAAG GAGACGTGAG ACATCAATCT 840
ATACACGTAA GATGTCCATT AGTCATTCAG GAAAGGCAGG ACAACTCCAC GGGTGAGGGG 900
GGTTTCCAGT TCATAGGTAG ATAAGAGACA AAAGGTTGCA GTCTTTTGAG TCTCTGAGAA 960
|
