| Tag | Content |
|---|
EnhancerAtlas ID | HS034-09438 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr14:95693020-95694330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr14:95693054-95693064 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr14:95693054-95693064 | GGCACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65498 | chr14:95692846-95694115 | Pancreatic_islets |
|
| | 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 |
| GH14I095226 | chr14 | 95693299 | 95694214 |
|
Enhancer Sequence | TCCCATCCCA GCCTCTTAAA TAGTTGGAAC TACAGGCACG TGCCATCACG TCTGGTTAAT 60
TTTTTAAACT TTTTGTAGAG ATGGAGTCTC TCTGTGTTGC CCAGGCTGGT CTCAAATTCC 120
TGGGCTCATG CGATATCCTC CTGCCTTGGC CTCCCAAAGG GCTGGGATTA CAGGCGTGAG 180
CCACCATGAC CGGCCGAAAC CCGATTCTTA ATAAGCTTCC ACCCCGGCAT GAATTTCCTG 240
TTTACCTTTT TGTACTGGGG GCTTTGGCAA GGTTAGAGCA GCTGGTCTGG GTGCTGTCTC 300
TGCTCCTGGG TACAGGGGAA GGCTGGGCAT TCACATGGGA GATAGGATTA ATGGGGCATG 360
GAGCTCCTGA TGGGAGACAG GATTAATGGG GCATGGAGCT CCTGAGGCCA ACGGGAGGGT 420
GGCAGCCATA ACCAGCCAGA GACCCAGGGG CAGGAAACAG TGGAACTGTG GCCCAGCCAC 480
CCTTTCCCTG TGGGAAAGCC TCCTTCCCGT GGCAGCCGTG GAGGGCCTGT GTTTCATTTT 540
TTATGGAGGA AGGTGGCATT TCCTTACCCT TTATACGAGT CCCTTTACCC CCAGTTAGTC 600
AAAATACAGG GCAATTCCAC CCGCAGGTGC ACAGAAAAGG GCTTCGCTTC AAGGGCAACA 660
GCGACTTTGA ACCAAAAGGC AAATTATTTT CTTTGCAAAC TGCCGCAGCT CCTTGGGCAC 720
CTTCCACCCT GAGCATGACG GGATCAGGTT ACTGAGGCTC TTACGGAAAT GTTATTCCTG 780
TTAATGCGAG GCAGAAAACG CGAGACCCGA ACGGAATACC CCCTGATAAA TGGACTAACA 840
ACATTTCCAG TTACCAGCCC CGGCCGTGGC CAAGCCTTAC TTCTGAGTTA AACCTGAAGA 900
ATAATTTCCA TTGACAGTTC CTATAAGAGC CTCAGCAGCA GCAGCAAACA GGGCCTTGGC 960
CGGAGTCCAT CCTGCGAGAT GGCAGGGGGA GAAATTGAAC CTGCGCCAGG GAAAACACTC 1020
CTTGGGCCCC AAACGCTCTG TGGGCTTCAT GAGATTGGTA TGGCCGAATA AACAGCACCC 1080
CCAGGGCTTT CTTCATGATC TAACTCCTTC GGTAAATTAA GGAATTTTTC CAGAAGCCAG 1140
AGACTCAGTA AATATTTCTG ACAGCCTTCA AATTGCAGTT AAGCCCAATT CACCAAGGAG 1200
TTCCTGGGTT TCCTTTACAT GCAAGGTTGT TCTTGAAAGT CTCAAGGTTG GAAACGTGGC 1260
TGTTAATTTT GCCCTGTTTA TTAGACATCA GTTTCAGGTG CTATCTGATT 1310
|
