| Tag | Content |
|---|
EnhancerAtlas ID | HS147-41146 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr8:120128460-120129670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr8:120128984-120128998 | AAAAAGGGGAAGTG | + | 7.03 | | SPIB | MA0081.2 | chr8:120128986-120128998 | AAAGGGGAAGTG | + | 6.07 | | SPIC | MA0687.1 | chr8:120128984-120128998 | AAAAAGGGGAAGTG | + | 6.02 | | Sox3 | MA0514.1 | chr8:120129425-120129435 | AAAACAAAGG | - | 6.02 |
|
| | 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 |
| GH08I119116 | chr8 | 120128394 | 120129260 |
|
Enhancer Sequence | AAGCCATAGT TGTTGAAGAA TATCCTCACA TTTTGCAGAA GTGTAATTAC CACATACCCA 60
TTGGGATTAT AGATTCACAG CTTCCTTACT CTTAACATGG CTTTTTCCTT TGACATCCAA 120
TAATCAAGGG TAAAAGGCAA ATTCATCTGT TTTGTGCTTA GATCACTAAA AGTTAACTCA 180
CTCTCATTTA GGTTTATGTG CTCTTATTCT AGTGGATCTT GGAGGGAACC TTTAATCTAC 240
TGAATCTCCT TCCCATGAAG CTCAATAAAT CCTACCTCAA TTCACCAAAA CTGGACAAAG 300
TGCTGTTTTA ACTGGTGTCC CAGTGTATCA GCTGGCTCTT ACACTGCTAT AAAGAACTAC 360
CTGAGACTGA GTAATTTATG AAGCAAAGAG GTTAAATTGA CTCACAGTTT TATAGGCTTT 420
ACAGGAAGCA TGGTTGGGGA AGCTTCAGGA AACTTAACAA TCACAGCAGG AGAGCAAAGG 480
GGAAGCAAGC ACTGTCTTCA CATGGTGCAG CAGGAGAGAG AAAGAAAAAG GGGAAGTGAC 540
ACATACTTTT AAACAATCAG ATCTCCTGAG AACTCACTCA CTATCGTGGG AACAGCAGCA 600
AGGAAATCTG TCCCCATGAT CCAATCACCT CCCACTAGTT CCCTTCCCCA ACATTAGGGA 660
TTACAGTTCA ACATGAGATT TGGGTGGGGA CACAGAGCCA AGCCATATCA TTCTGCCCCT 720
GGCCCCTCCC AAATCTCATG TCCTTCTCAC ATTTCAAAAC CAATCATGCC TTCCCAACAG 780
TCTGCCAGAA TCTTAACTAA TTCCAGCATT AACTCAAAAG TCCAAGTCCA AAGTCTTTTC 840
TGAAACAATG CAACTCCCTT CTGCCTATGA GCCTGTATAA TCAAAATCAA GTTAGTTACT 900
GCCAAGATAC AATGGGGGTA TAGGCATTGG GTACATGCTA CCATTCCAAA AAGGAGAAAT 960
TGGCCAAAAC AAAGGGGTTA CAGGCCCCAT GTGAGTCCAA AACCCAGCAG GGCAGTCATT 1020
AAATCTTAAA GCTCCAAAAT AATCTCCGAC TCCATGTCTC ACATTCAGAT CATGCTGATG 1080
CAAGGAGTGA GCTCCCAAGA CTCCACCTCT GTGTCTCTGC AGGGTACAGG CCTTGCAGCT 1140
ACTTTCACAG GCTGGTGTTA AGTGCCTGTG GCTTTTCCAG GCACATGGTA CAAGCTATCA 1200
GTGAATCTAC 1210
|
