Tag | Content |
---|
EnhancerAtlas ID | HS034-28019 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr7:75719000-75720390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:75719973-75719988 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr7:75720099-75720114 | GCTGGCCTTGAACTC | - | 8.25 |
|
| 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 |
GH07I076086 | chr7 | 75715336 | 75720188 |
|
Enhancer Sequence | CCCAGACTGG TCTTGAACTC CTGGGTCAAA CTAATCCTCC CGCCTTCGCC TCCGAAAGTG 60 CTAGGATTAT AGGCTTTAGC CACTGTGCCC AGTCTATTTA TCTTTCTATA ACTCATATAT 120 TAAATCTTCC TCCTTAAATC ACCTCCTACC CACCCATCTG CAGGGATAGC AAACACAGGT 180 CTCAGCAGGT CAGGCAACCT ACAGGAGGGA ATGAGGCCAG AGTAATGTGG GAGACCAGGG 240 GGAACTGTAG CAAACTGCAA GGTATTCACT TCAATAGTTC TTCAACACTG TGATGGTCAA 300 ACCAAACACA GAAACAGGAA GCCCAGTTCA GTCGCCAGCA GCCAATGTGG GATATTTGAT 360 CTACATGCTA CAGGGCAAAC TGCTTACGAT AAATGACCTG GTCTCCACCA ACCTGCTCTT 420 CAAGTCCAGC CGCTCCTGCC CAACTCCCTA CACTCTACTG ACACGACCCA CATTCACAGT 480 ACTCTCCTGA AACTTTGCTT GTTCACTCTT TTTTTATTTT CCCAATGAAT ATTTCTTTTT 540 CTTTTTTTTA CTTTTTTTGA GACAGAGTCC CCTTCTGTTA CACAGGCTGA AGTACAGGCG 600 GATGATTATG GCTCACTGCA GCTTCGTTAT GGCTCACTGC AGCTTCCGTC ACCTGGGCTC 660 AAGTGATCCT CCCACCTTAG CCTCCCAAGT AGCGGGGATT ACAGTCATGT AACACCACAC 720 CCAGCTAAAT TTATTATTTT TTCTTGTCTT TTTTTTTTTT TTTTTTTTTT TTCAGACGGA 780 GTCTCGCTCT GTTGCCCAGA CTGGAGTGCA GTGGCATGAT CTCAGCTCAC TGCAACCTCT 840 GCCTCCTGGG TTCAAGCAAT TCTCTTTCCT CAGCCTCCCG AGTAGCTGGG ATTACAGGTG 900 CATGCCACCA TGCCTGACTA ATTTTTATAT TTTTAGTAGA GATGGGGTTT TACCATGTTC 960 ACTAGGCTGG TCTTGAACTC CTGACCTCAG ATGATCTGCC CACGTCGGCC TCCCAAAGTG 1020 CTGGGATTAC AAGTGTGAGC CACCGTGCCT GGCCAGTTTA TTATTTTTTC TAGAGACAGG 1080 GTCTCACTAC GTTGCCCAGG CTGGCCTTGA ACTCCTGGGC ACAAGCAATC CTCTGGCCCC 1140 CACCTTCCAA AAAGCTGGGA TTACAGGCTT GCGCCAACAC ATCAGGCCCT AACAAACACT 1200 TCTTGAGCTC CTACTATATA CCAGGCACTA TAATAGGTGC CCAGGAAACA GCGGTGAACA 1260 AGGTATAACA GTTTCTGCCC TTGGCCGGGC GTGGTGGCTC ATGCCTGTAA TCCCAGCACT 1320 TTGGGAAGCC GAGGCCGGTG AATCACCTGA AGTCAGGAGT TCGAGACCAG CCTGACGAAC 1380 ATGGTGAAAC 1390
|