| Tag | Content |
|---|
EnhancerAtlas ID | HS145-12864 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:86181900-86182670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr2:86182140-86182152 | TTCTGTTTACTT | - | 7.22 | | FOXP2 | MA0593.1 | chr2:86182141-86182152 | TCTGTTTACTT | - | 6.32 | | Gata1 | MA0035.3 | chr2:86182306-86182317 | AGAGATAAGGA | - | 6.02 | | Nkx3-2 | MA0122.3 | chr2:86182326-86182339 | CTTAAGTGGTTAA | - | 6.5 | | ZNF263 | MA0528.1 | chr2:86182592-86182613 | CTTCTCCGCTCCTCCTCCTCC | - | 7.32 |
|
| | 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 |
| GH02I085954 | chr2 | 86182101 | 86184793 |
|
Enhancer Sequence | GTTTCAATAG CCAGTGAGAG TGAGCCATGG AGAATAAAAA TGTACAAGTA AACAGTCGTT 60
CCACTTATAC ACAGTTAAGG ACTTGTGGGA GGGGGGCAAG TTCCAGTTTT TCAACATAGT 120
TTCTGATTGA AAGTGCCATT GTAACCCTCA TTATGGCCAC CAGCTTAAAT TTGAGGGCTC 180
CCGTTGCCCT GGAATAAACC CCTAGTTTTC AGACTTCCTG GAGCCACCAT CCTTCATCTC 240
TTCTGTTTAC TTTTTTCTCT TCTGTTTAAA TTGGAGGGCC ATTTATGCCC TCCCCTTCTC 300
CTTGCTGAAG TTGTGTACAC AATGACTGGC ACAGAGGTGT TTCTACCTGC ACAGGCTCAT 360
GACATTCTCA CAGTCAGCCC ATAGATCGGT TTCTTCTCTC AATCTCAGAG ATAAGGAAAC 420
TGAGGTCTTA AGTGGTTAAG TCATTTGTCC CAGGTCGCCT GGCAGCAAGT TGTACCCACA 480
GTGCTAGCCA ATGTCTCGCT GACATGTGTG GGCACCACAT GGGCCCATCC ATGGTCAGGG 540
ACTTTTCCTG GCTCTGCCCA TAGCATCCTC ATTCGTCTTG TTTGCTTATA TGTTTCTTAC 600
AACTACCTCA CAGCCTCAAC CATGTCTTTA AAATTATTCA ATTATTCATA GAGCTGGATT 660
TACAAGTCTA GGTCTCCTTC GTCAGGGGTG GCCTTCTCCG CTCCTCCTCC TCCTCTCTGG 720
AGGTGGTTTC ATCACAGACT GTAAAGGTTC TGTAAAAAAT AATCTAGTCC 770
|
