| Tag | Content |
|---|
EnhancerAtlas ID | HS146-09066 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:240551670-240553060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr2:240552348-240552359 | AAAACAAAGAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_39642 | chr2:240550741-240551903 | Jurkat | | SE_66548 | chr2:240550741-240551903 | Jurkat |
|
| | 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 |
| GH02I239629 | chr2 | 240551657 | 240553370 |
|
Enhancer Sequence | TGAAACGTCA GAAACCCTCC AGAGAGCATA GGTTGCCCGG GCGACTGTAG TACAGCATCA 60
AGGCACCCTT GAGTTGGCAA GACACAGGCT TGCTGTGCCT GAGAAGCACA AGGTTCCACT 120
TCCCAGCCAT GGTGGTTTTC AGCAGTGCTG TTTCTACTCT TAGGTCAGAA CAGAGATATG 180
GGAAAAATCC CTGCTCTTCT GTTTCTTTTC CCCAGTGCCG CCTCCTCCAG CCTCCAATGG 240
AGGTGTTTCC ATGGGTGACC ACATTCTGTT CCACTGGTGG TGGCCTTTGT GTGAGTGCTC 300
CTTCAGGGAC CACATTGATC ATTAACACAC CTTTGAGGTT TCTTTCTTTT TTCTCTGAAA 360
CATGGCTTCT TAAAAACTTT ACACTTTTTC TCTCATGAGC ATTTTAACAC ATTTAAAAAA 420
TAACAGAACA GTTAAAAAAA AAAACCCACA GTTTCACACA GGCTTCTTCT CACTGAATCA 480
TGTTTCATCT TTTCCCTTGG CACAACCAAA GGGAAGGTTA ATTTAAAACA GCTGAGAGTG 540
ATGTCACGTC ACACGCCGAC ACCTCTTTTT CTTTTTTTTT TTTTTTTTTT TTTTTTGCCA 600
GGAAAGAAAA GAGGTTCACC TCAGGCTGCT CAGAAGGAAG GTGTTCCAGG AAGGCCAGAA 660
AAGGGAGGCT GCTCTGGAAA AACAAAGAAG AGCTTGGCAG GTCCTAGAAC GGAGGAGAAG 720
TTAGACCCTG GGAATCCAAG ATGCTGCAAC GTCAGGCAGC TGGTCCCCAG CAAGGCTGGC 780
ACGTGGAAAC CTCACGGAGA AAAGTGATTC ATAACCAAAG CAGGGCTCCC ACAGCGACGC 840
TGAGCAGACA CAGAACTATT TTTCACATAA CACTTATTTT ATTTAAAAAA AATGTTAAAT 900
GACTTTCCTT TGCATGGATT CTCTGTTTCT CTTGCTCTGG TTCTGGAAGC CATGTGGAGT 960
GGTGGCCAAG AGTCAGTCCT GTTCTGTATT TTTTTGTTGT TGTTGTTATC TTTCTGAGTT 1020
GATCAGCAAC TGAGAGAATT GAGGAAAGTC GCCCAGGTGG CTCATGTCCA GTGCGTCACT 1080
CCACCCCATT CCGACAGCCT CATAGGTTGC TTAACTCTGG AGCCTGGCAT TCTCCAGATG 1140
CCCCTGCAGG GAGGATTACT TGGCTCCCTC CAGCAGACAA CCTTGTGGAA CGCTCAGAGC 1200
AGAAGTGAGT CACTGCAGCA GGCCCTGTGC ACGGAGGCAA GCCAGGAGGT GGTGGAGCTT 1260
TATGCGTCCA TCATCAGCAT TAAAGATGCA GCGAGGGGCA GGGCTCCTTC CCCCAGAACC 1320
ATGCATGGTG GGCTATTTGT CCCCAAGTGT GATCTTTGCC TGCAAGGTTC CTGCTGTTGT 1380
GGCACTCAGA 1390
|
