| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00373 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:24867560-24868750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:24868647-24868666 | CTGCCTCCAGGGGGCGCCA | + | 7.37 | | FOXF2 | MA0030.1 | chr1:24867961-24867975 | GAAAGGTAAACAAA | + | 6.79 | | ZBTB18 | MA0698.1 | chr1:24868159-24868172 | ACACATCTGGATG | - | 6.78 | | ZNF263 | MA0528.1 | chr1:24868079-24868100 | CCCTCCACTTCCTCCTCCATC | - | 7.28 | | ZNF263 | MA0528.1 | chr1:24868076-24868097 | CCTCCCTCCACTTCCTCCTCC | - | 8.97 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_17366 | chr1:24865116-24868450 | CD4p_CD25-_CD45RAp_Naive | | SE_18454 | chr1:24865205-24868608 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_28444 | chr1:24865846-24868996 | Fetal_Intestine | | SE_29333 | chr1:24865693-24868969 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024539 | chr1 | 24866152 | 24868897 |
|
Enhancer Sequence | TATTTTCAAT ACGCATCACT TACATTTAGC TAATAAGACA GAGAAGTGCA ATATTGTGTT 60
TGTTCCTTTC ACAAGAGTCC TGTTGAACAT TAATGCCGTG CAGTGCCAGA GTTCAAGGTG 120
GTGAGTCACT GCTCACTCTG TAAATAACCA CTGCACTTTC AGCTCTTCCC CAAGAAACCT 180
TTTACCCTGG TTTCCCCTTT GGTTAAAAAT GATTTATTCC GGGTAAAGAC TTACTTTTTG 240
TCTCGGTTAA AAAAAAAAAA TCTCCAAAAT GTGGAACTAT AAATGACAGT AGAGGTTATC 300
TAGTGCAGTG GGATTTCGAA TACTTATTTT TAAGCCATAG GACTCTGCTC TTTGTTCAAA 360
TGAAATCTTA CACAAAGCCA ATGTAAAACT ATTACAAAAA GGAAAGGTAA ACAAAGCTGC 420
TCCTTTTCAA GGGGCTGGGG GAAGAATGGG GACCTGAGTT CAACCCCTGT GAGAGCTCAG 480
CAGAACAGAC CCAGACACAC CCCTCTATTG CCCCTGCCTC CCTCCACTTC CTCCTCCATC 540
CCAACCCCAC CCCCAACACA CCTTTACAAG AAAGTGGCCC CAGAGGCATT GCCAAATGCA 600
CACATCTGGA TGGTCATGGA CCTGGGACTA GAACCCATTT CTTGACATTC TTTCTACCAC 660
ACTCCACTAC TTTGTTACAC CAAAATCTAA TTTTTCTGGA TAAATGTATC TGGATAAAAA 720
GGTTCTTGAT ATTGTTTTGT TTTTGAGACA AGGTCTTGCT CTGTCGCCTA GGCTGGAGTG 780
CAGTGGCATG AACACAGTTC ACTGCAGCCC CAACCTCCCA ACTCAGTCTC CGAAGTAGCT 840
AGGATGACAA GTGTGCACCA CCACACCCGG CTAATTTTTG TATTTTCTGT GGAGACAGGG 900
TTTCCCTATG TTGCCCAGGC TGGTCTCTAA TTCCTGATCT CAGGCGGTCC ACTTGCCTTG 960
GCCTCCCAAA GTGCTGAGAT TACAGGCATG AGCCACCGAA CCTGGCCTTT TTTGTTTTTA 1020
AAAAACTAAA GCGGAGTCGC TGAGGACATT TCCACTTTGA AGTTTTTCCA AGCTGTGTTC 1080
TGTGGGGCTG CCTCCAGGGG GCGCCATGCT TCCAGGTTCC TGGGGCCTTT CACTCCTGCT 1140
TCAACTCTCC TATTATTTGC TATACCTAAA GGTCCTAGCA TGTTTTCCAC 1190
|
