| Tag | Content |
|---|
EnhancerAtlas ID | HS037-07309 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:106827050-106828550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr11:106828256-106828269 | AGGGGCTTCCCCT | - | 6.02 | | SP1 | MA0079.4 | chr11:106827728-106827743 | GAAGCCCCGCCCACT | + | 6.79 | | SP2 | MA0516.2 | chr11:106827727-106827744 | GGAAGCCCCGCCCACTG | + | 6.76 | | SP4 | MA0685.1 | chr11:106827728-106827745 | GAAGCCCCGCCCACTGA | + | 6.56 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I106956 | chr11 | 106827528 | 106828265 |
|
Enhancer Sequence | CATTGTAATC ATTTGGAGAT GAAGCACTCT GGCCTTTTGG GTTTACAGCA TTTTTTCATT 60
GATTCTTTCT TACCTTCCTC AATTTGTCTA CTTTCAGTCT TTGAGCCTGC TGATCCTTGG 120
ATAGGGTTTT TTGTGGAGGC CTTTTTGTTG TTGTTGTTGT TGTTGATGCT GTTGTCACTT 180
TCTGCTTGTT TTTCTTTCAA TAATTGGTCC CTCTTCTGTA GGACTGCTGC AGTTTGCTAG 240
GGGTTCACTT CAGGTCGTAT TCATGTGATT CGCTCCAGTT CCTGGAGATG TCATTCAAGG 300
AGTCTGGAGA GCAGTAAAGA TGGGTGCCTG CTCCTTCTTC TGGGACCTCT GACCTCGACA 360
GGCACCAACC TGATGCCAGT AGGATGACTC CTGTATAGGG TGTCTGACAA CCCCTGTTGG 420
AGGGTCTCAC CCAATCGGGT GGCACAGGGA GCAGGACCCA TTTAATGAAG CACTTTGTCC 480
TTTGGTGGAG AGGGTATGTT TCACTAGGGG AAAACCCACT CATCTGAGCT GCCTGGATTT 540
CTCAGAACTA CCAAGAGGAG ACAGCAAGTC TGCTGGTCCC CAGAGACTGT GGCCATCCCT 600
CTCCCTAGGG ACTCAGGCCC AGGGAGATCT GAATTCTGTC CCCGAGCCTC TAGCTGGAGT 660
TATTGGAGAT CCTGCAGGGA AGCCCCGCCC ACTGAGGAAT GATGGGTTGG GATTAGGCCT 720
GAAGAGGCAC TCTAGCCGCA GACTGCCACA GAGGGTGTGT TGGGCTGTGG GGACAAGTCT 780
TGGGAGCAAG TCGTCCAGCC TCCCTGGCTC TAGCTCTAGC AGGGGAAAGT ACAGCCTGGA 840
GCTATAGAAA TGGGTGTGCC CACCCTGCCC AGGGAGCTTA GTGTGTTAGG CAGTTGCAAG 900
TCCCAGTGCT GACTCTTGCC CCTCCCCCCA GGAGCTCAAA TGGCTTAGAC AGCAGGCAGC 960
CACAGCTGGT GCTGGTTGCC TCTTCTTCCC CCCTCCCCAC CAGCAACCCC CACTTCCTGA 1020
GTTCCATAGG CTTAAGCAGA CTCCAGCTGA GAGGCTGTAA GAATCTGCAT GTTCCAAGGC 1080
TGGGACGCTA GGCCCTGGTG GCGTGGGTTC ACGAGTGGGA TCTTCCAATC CATGGGTGGC 1140
AGGGTTCTGT GGAAAAAGCA GTTTCCCTAG CGCACTCACT CACCACCGCC TCCTTTGGCT 1200
TGGGGAAGGG GCTTCCCCTT CCCCGTGTGG CTCTCAGGTG GGCCTTCTCA CTACACTGCT 1260
CTTCCTTCTC TCTGTGGTCA GGCCAGCCTT CTTGTCAATT TTGGCGAGAG AACCTGAATA 1320
CCTTGGTTGC TGATGAAGGA TTCACATGCT TAGATTTTTT TTCCAGTGGG AGCCTCTGAA 1380
CACGCAGCTT CCAGTCGGCC ATCTTGGCCC CGCCTCCAAA AAAAATGGTC ACTTTTTTTT 1440
TTAAATCACT AAATTGTGAT TCACCCTCCT CAACTGCTCC AACCAAGTGT TGGGAGCTAT 1500
|
