| Tag | Content |
|---|
EnhancerAtlas ID | HS148-14901 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:148845460-148846610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr5:148846350-148846364 | TGTGCGTGGGCGGG | - | 6.53 | | EGR2 | MA0472.2 | chr5:148846352-148846363 | TGCGTGGGCGG | - | 6.32 | | EGR3 | MA0732.1 | chr5:148846350-148846365 | TGTGCGTGGGCGGGA | - | 6.9 | | EGR4 | MA0733.1 | chr5:148846349-148846365 | CTGTGCGTGGGCGGGA | - | 6.71 | | Nr2f6(var.2) | MA0728.1 | chr5:148845568-148845583 | TGAACTCCTGACCTT | - | 6.04 | | SREBF2 | MA0596.1 | chr5:148846251-148846261 | ATGGGGTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23396 | chr5:148845540-148846729 | Colon_Crypt_1 | | SE_24335 | chr5:148845695-148846582 | Colon_Crypt_2 | | SE_37458 | chr5:148843696-148847073 | HSMMtube | | SE_50445 | chr5:148845520-148846757 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I149466 | chr5 | 148845585 | 148846772 |
|
Enhancer Sequence | GCCTCAGCCT CCTGAGTAGC TGGGATTACA GGTGCCTGCC ACCACGCCTG GCTAATTTTT 60
TGTATTTTTA GTACAGACAG GGTTTCACCA TCTTGGCCAG GCTGGTCTTG AACTCCTGAC 120
CTTGTGATCC ACTCGCCTCG ACCTCCAAAA GTGCTGGGGT TACAGACATG AGCCATCACA 180
CCCGGCCAAC TCCTGCATCT TTTAGGGCAG GGAGATGTTC AAGCCATAAC ACCGCCTCAC 240
AGGATTGTCA AATGGATGAA ATGAGCTAAC GCATGCTGTG CCAGGCACAA AGTCATCACT 300
CAGTGAATGT TCTTTATTAT CATATTGTTA TTATTTCTCT GCACAGTGGC TGCCAGTGTG 360
CTGCACTGGG TCCTATGGGG TGGCCATCCC AGGGTAGTGC AAGTGCCCCA CAAATCCCTG 420
AAATGTGACC AGCAGTGGCT CCAGAATTTC ACAGTAAGGA GGAACTTGGG GGCGTGGGAG 480
GGAGATCAGG TTGGAAGGGG CTCAGCACGC TCACTGATGG ATCTAAGCTC TCATATCACA 540
CGACGAAGAC AGCAGTGCTT CCTGAAGATG CTCTGAGTCC CACTGGGTGC GTGACTGAGA 600
AACCGCGCAG CTGTCCACCT GTGTCAGATC CTATCGCTGC TGTTGTAAAT CCTTAGCGAA 660
GCTTGTAGGG GAAGTGACAG TCATTGCTGG TGGTGAGTCG GGTGACTGAT GTGCTCCCAA 720
GGCTCTCCTT GATACAGGCA CTTCATGCAC CACGTCATCA TGCTAGGCTA GTAGTCCCAG 780
GAGGCTGAGT CATGGGGTGA TGTCGGGATG CTCCCCTCGG TGGGGCTGTG TCTTGTGAGT 840
GGTCGCGTTG GTGGGGATGG CGGCTCTCTT GCTGGGAGGC AACAGACCTC TGTGCGTGGG 900
CGGGAGGTGG CACAGGCTTC TCATCTGGGA GACCAGATTG AATCTCAAAT TGCTGCCTGC 960
CTTCCGCACT TAAAACTGCT TCCTCACTCA GCACTTTGTG AGTGAGGCTC AAGTTCAAAG 1020
TCCTGAATGA AAGCCTTGAT AATGAATCTG ACCCGACGAT GATACAAAGC TTCAATTATG 1080
GAGCTTGTAA AATGATACTG ATATATGTGT GCTTCCTTGC ATTTCTTCTG GGTTTCGGTT 1140
GTTCCCCTGT 1150
|
