| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13842 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:113381650-113382960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:113382866-113382881 | TGAACTCTTGACCTT | - | 7.36 | | RARA | MA0729.1 | chr2:113382863-113382881 | TCTTGAACTCTTGACCTT | - | 6.24 | | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I112621 | chr2 | 113379040 | 113390802 |
|
Enhancer Sequence | TCATAAAAGC TTTATCATGC ATCAGAGCTA TCCGGAAGGC TTTTTAAAAC ACAGATTGCT 60
CAGCTGGGCG CAGTAGGGTG CGCCTGTAGT CCTAGCTACT TGGGAGGCTG AGGCAGAAGG 120
ATCTTTTGAG CCCTGGAGTT TGAGGCTACA GCATGCTATG ATTGTGCCTG TGAATAGCCA 180
CTGCACTCCA GCCTGGGCGG CCTAGCAAGA CCCTGTCTCT AAAACAATAA CATCAACTAA 240
AACAAAAACC ACGCAGATTG CTGGACCCCA ACCTAGAGTT TCTGATCCAG TAGTATTGGG 300
GTGGGGCCTG AGAATTTGCA TTTCTGACAA GTCCCCAGAT GATGTTGATC CTTATTCTCC 360
TGGCCCATAG ACCACTTAAT TAAAGCCAGC AAAGTAGTCA TCAACGTTGA CCCAGGATAT 420
AAGCTGAAGA TGATGAACAG CCTTGAGGCA GTAAGGGAGG CCTGCCCTCC AACATCAGGA 480
AGCCAAGTGA AGGCGTGACT CACCAGGGCA GGGTGGGGTT CCTGCGTGTG AGAAACCAGA 540
ATTGAGAGCT GCACCAGCTG TGTGGCCCCA GGTTTCTCAG GGTGAGGAGA GGCAGCCCAG 600
GGGAAAGGCA CTCGGGACCA CACCCCAACT CACCTACCCT GTGTAAGTTT TTTCCATTGC 660
ATGTATCAAC ATCTAACATG TCATATATTT GATTTACCTC ATTTATTCTC TGACTCCTTG 720
CCTCCTGTTA GAATATAGGT TCTCTAGAAC AAGGATTTTT ATATGTTTTA TAGAAGAACA 780
GTAACTGAAT CATAGCAGGT GTTCAAATAC TGACTGAATG CATGCCTATA TACATATAAC 840
TATGTTCATG ATACTGTTTC TAGAAGGATC CACAAGAAAA TGGCAGCAGA CTGTCTCTGG 900
GCAAGGGAAA TGGAGGAATG GGTGGGGCAA CTAAAACTTT TTACTGACTC TATAGCTCTT 960
TGAATTTTTC CTTTTTTTTT TTTTTTTTTT GAGATGGAGT CTTGCTGTGT CACCCAGGCT 1020
GGAGTGCACT GGCGCAATCT TGGCTCACTG CAACCTCTGC CTCCGGGGTT CAAGCAATTC 1080
TCCTGTCTCA GCCTCCCGAG TAGCTGAGAT TACAGGCATG CATCACCATG CCCGGCTCAT 1140
TTTTGTATTT TTAGTAGGGA CAGGGCGGGA GTGGGGGAGG GTTTCACCAT GTTGGCCATG 1200
TTGGCCAGGC TGGTCTTGAA CTCTTGACCT TGTGATCCAC CCGACTCAGC CTCCCAAAGT 1260
GCTGGGATTA CAGGTGTGAG CCACAGCGCC CAGCCGAATT TTTCCTATGT 1310
|
