| Tag | Content |
|---|
EnhancerAtlas ID | HS176-21448 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:113381460-113382690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr2:113382443-113382453 | AGCAGGTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_36149 | chr2:113381310-113386820 | HMEC | | SE_38814 | chr2:113381522-113389910 | HUVEC | | SE_46500 | chr2:113381322-113386057 | Osteoblasts | | SE_55939 | chr2:113381435-113390227 | u87 | | SE_65225 | chr2:113381001-113383847 | NHEK | | SE_67655 | chr2:113381435-113390227 | u87 |
|
| | 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 |
| GH02I112621 | chr2 | 113379040 | 113390802 |
|
Enhancer Sequence | CTTGATTCTT ATTTTCAAAT AATTGGGCTG TAAGATTTAT CTGTTACTTC TTAACATATA 60
ATTTGTACAC CTGTCTAGGA TTTAACTTGG AAAAGATTTT TCAAAACTTG GTACGATTAT 120
ATAAAATGTG TGCTTATGAC CATAGCTGGT AGGCATGTGA GATGGTAAGG CATTTCCGCA 180
GAGCAGAGGT TCATAAAAGC TTTATCATGC ATCAGAGCTA TCCGGAAGGC TTTTTAAAAC 240
ACAGATTGCT CAGCTGGGCG CAGTAGGGTG CGCCTGTAGT CCTAGCTACT TGGGAGGCTG 300
AGGCAGAAGG ATCTTTTGAG CCCTGGAGTT TGAGGCTACA GCATGCTATG ATTGTGCCTG 360
TGAATAGCCA CTGCACTCCA GCCTGGGCGG CCTAGCAAGA CCCTGTCTCT AAAACAATAA 420
CATCAACTAA AACAAAAACC ACGCAGATTG CTGGACCCCA ACCTAGAGTT TCTGATCCAG 480
TAGTATTGGG GTGGGGCCTG AGAATTTGCA TTTCTGACAA GTCCCCAGAT GATGTTGATC 540
CTTATTCTCC TGGCCCATAG ACCACTTAAT TAAAGCCAGC AAAGTAGTCA TCAACGTTGA 600
CCCAGGATAT AAGCTGAAGA TGATGAACAG CCTTGAGGCA GTAAGGGAGG CCTGCCCTCC 660
AACATCAGGA AGCCAAGTGA AGGCGTGACT CACCAGGGCA GGGTGGGGTT CCTGCGTGTG 720
AGAAACCAGA ATTGAGAGCT GCACCAGCTG TGTGGCCCCA GGTTTCTCAG GGTGAGGAGA 780
GGCAGCCCAG GGGAAAGGCA CTCGGGACCA CACCCCAACT CACCTACCCT GTGTAAGTTT 840
TTTCCATTGC ATGTATCAAC ATCTAACATG TCATATATTT GATTTACCTC ATTTATTCTC 900
TGACTCCTTG CCTCCTGTTA GAATATAGGT TCTCTAGAAC AAGGATTTTT ATATGTTTTA 960
TAGAAGAACA GTAACTGAAT CATAGCAGGT GTTCAAATAC TGACTGAATG CATGCCTATA 1020
TACATATAAC TATGTTCATG ATACTGTTTC TAGAAGGATC CACAAGAAAA TGGCAGCAGA 1080
CTGTCTCTGG GCAAGGGAAA TGGAGGAATG GGTGGGGCAA CTAAAACTTT TTACTGACTC 1140
TATAGCTCTT TGAATTTTTC CTTTTTTTTT TTTTTTTTTT GAGATGGAGT CTTGCTGTGT 1200
CACCCAGGCT GGAGTGCACT GGCGCAATCT 1230
|
