| Tag | Content |
|---|
EnhancerAtlas ID | HS106-02198 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr8:121060010-121061180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr8:121060068-121060083 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr8:121060068-121060086 | GAGGTCAAGAGTTCAAGA | + | 6.45 | | RORA | MA0071.1 | chr8:121060660-121060670 | TGACCTTGAT | - | 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 |
| GH08I120047 | chr8 | 121059808 | 121061165 |
|
Enhancer Sequence | GTGGTGGCTC ACACCTATAA TCCCAGCACT TTGGGAGGCC AAGGTGGGAG GATCACCGGA 60
GGTCAAGAGT TCAAGACCAG ACTGGCCAAC ATGGCGAACC CCCTCTCTAC CAAAAATACA 120
AAAAATTAGC TGGGCATGGT GGCACACACC TGTAATCCCA GCTACTCGGG AGGCTGAGGT 180
GGGAGGATCG CTTGAGCCTG GGAGATGGAG GAGATCGTGC CACAGCACTC CAGCCTGGGC 240
AACAGAGGGA GACTCCATGT CAAAAAAAAA AAAAAGTAAA TGGTGAAATG TGATCCCTGA 300
GCGATGCGGA GACATGGCTA ATCTCAGGGA GCCTGCGAAG GGTCAGCTGG AGAGGGCACT 360
CACCTGGCAA CTCCTGCCCT CTTATTTGGC AGTGCAAAAA GGCTATTCAT CTTTTTGGAA 420
AAAGAAACCC CTGTATCTGT GGAAAAGACA AGGGATTTGA AATTTCCAAG TCTAGGGTCT 480
AAAGCTCTGG GTTGGGAAGG AGGTGAAATT CTTCTCATTC TTTGGCTCAT GAGTCTGCTG 540
CAGCAGAAAA AAACAAAGCC CAGGCTGATG CCTGCTAAAT TGCAAATTAC TGCTAAATTG 600
TCTTGCAAAT TACTGTGGCC TAGTTCAGGA TAGATTGTGA CCTGTTTGTG TGACCTTGAT 660
TATGACTGTG ACCTCCACCA TGGTTGAAAA CTGCTGATTT TGTATAAGAT GTACCCTGAA 720
TCCATGAAGA CAAATTTGTG GAACCAAGAA AAGAGAAACA GTAATAGTGT GATCTTATGT 780
GGAGAAAACA CCCTAGTAGG TTGGGGAGTG CAAAGTATCA AGGTTTATGA CAACAGCGAG 840
TGTTTATTGA GTAAATAAGC AGTCTGTGTA CTACTGCCCG CTTTCCATTT TGTTTTGCCT 900
GTGACCGTGA AAGAAGTGGG TATTTTTTGA AAGGAAAGAG ATTAATAGTA CTCAGCATCG 960
GTGTAGTGCT TGGTGTTTGC AAAGAGGTTT CAAATGCACT ATCTAGTGTG AGCCTGTGAG 1020
AATAGGCGTT TTTACCTGTT GTACAAGTGA GGCATTTATA TCGTTGAAAC ATAGAAGAGG 1080
AGAAATTACT TGATTAATGT ATTCCACCAA AGGGACCTAT AACTTAAATC TGTATCTTTG 1140
ATTCTAAGTC CCCTCATCTT TTCCACAGTG 1170
|
