| Tag | Content |
|---|
EnhancerAtlas ID | HS060-31746 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr7:66593360-66594690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:66593389-66593401 | CTCTGTTTACAT | - | 6.32 | | FOXP2 | MA0593.1 | chr7:66593390-66593401 | TCTGTTTACAT | - | 6.02 | | Foxa2 | MA0047.2 | chr7:66593392-66593404 | TGTTTACATTGT | + | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28329 | chr7:66592414-66596713 | Fetal_Intestine | | SE_29136 | chr7:66592645-66596610 | Fetal_Intestine_Large |
|
| | 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 |
| GH07I067127 | chr7 | 66592789 | 66596051 |
|
Enhancer Sequence | TCGATTTTGT TCTTTCTTAG GATTTCGATC TCTGTTTACA TTGTCTATCT GTTCTTGTGT 60
GCTGTGTACT TTATCCACTG GAGCCCTTTG CATCTGGTCG GGTTATCCCA ACATCCCTGC 120
CGTGTCAGAG CCTGGTTTGG ATCCTTGTGC TATCTCTTTA AACTTTGCTT TTTGCCTTTT 180
AGTGTGCCTT GTAACTTCTT GTCACTGAAC GTGATATCCT GGGTAAAAGG AACTGCTCTC 240
ACTAGACCTT TAATAATGTG ATGGTATGGT GTATGGGGAG GGGAAGCATT CTGTAGTCTT 300
ATGATTAGGT CTCAGTGTTT TTTTTTTTTT TTTTTGAGAC GGAGTCTTGC TCTGTCACAG 360
GCTGGAGTGC AGTGGCACGA TCTTGGCTCA CTGCAACTTC TGCCTCCCAG GTTCAAGCAA 420
TTCTCCTGCC TCAGCCTTCC AAGTAGCTAG GATTACAGGC ACCCGCCACC ATGCTCCACT 480
AATTTTTGTA TTTTTACTAG ATACGGGGTT TTACCATGTT GGGCAGGCTA GTCTTGAACT 540
CCTAACCTCA AATGATCCAC CTGCCTTGGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG 600
CCACCGCGCC CAGTCTAGGT CTCAGTCTTT TAGTGAGGCT GTACCCCTGG ACTGTGAACT 660
TCACAAATAC TTCTCAGTTT TTTCTTCCCC CTTGGGACAG GTTGGCTAGA GTGTGCTGCA 720
GTTGGCTATT TCCCTTTTCT TACATGGAAG GCCGGTGCTG GCTGGAGTTG GGTATTTCTC 780
TTCCACTTGG TTAGTTAGGC TCTGATAAAA CCAAGCAAGT TAGGTTCTGG TTAAATCGTT 840
TCTCCTGGGA GCAGACCTTG TTATCAACAG AATGCTCTGA CACATGTCAA ATGGTTCCTG 900
TTTCCCTCCC CTTACCGGAA GCACAAGGGA TTTCCCCCTG TATACTTACT GTGAGAATCT 960
GGCAGAGCTC CAGTAGGTAA AACTCACAAA AGTGTAGGGC CCCTAATGAC TGGGTCTGTC 1020
TGGAATTTTT ATGTGTCAGA CTTGTCCACA CTGAGCCTCC AGCACTTTGT CAATTACAGT 1080
TCAGTTTCCC TGTGTTAGCG CTGGTCTCTG TGGAGGTTTC TGCTCCTGTT AAGTTGTGAT 1140
TCTCTGTGCC TGCCTGTTTT TCCCTCCAAT TATGGGGACA GCAGGTTTGC CCTGTGACCT 1200
CACTTCTCTG ATGGATCTAA GAACAGTTGT TGATTTTTCA ATTTGTTCAG CTTTTTACTT 1260
GTTAAGACAC AGTGATGACG TCCAAGCAAC TTTCTTGCTG CATTGGAAAC TAGAAGGCTC 1320
GTAGGGGTTA 1330
|
