| Tag | Content |
|---|
EnhancerAtlas ID | HS146-08911 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:226979860-226981180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr2:226980382-226980402 | AATGGGTAACTTTCACCCAC | - | 6.19 | | Pou2f3 | MA0627.1 | chr2:226980936-226980952 | TAACATTTGCATAATA | - | 6.3 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_34253 | chr2:226977990-226990861 | HCT-116 | | SE_43429 | chr2:226978957-226987379 | MCF-7 | | SE_56369 | chr2:226978138-226987611 | u87 | | SE_64924 | chr2:226978854-226981139 | NHEK | | SE_67944 | chr2:226978138-226987611 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I226113 | chr2 | 226978250 | 226991855 |
|
Enhancer Sequence | GTAAAGTTGG CTCTGCTAGT ACACAGGGTA TTATCTTCTT TGTAATGCTT GCAAGAAGAA 60
GATCAAAAGT AGCTCCGATC TTCATCTTAA ACCATAGATT ATGAGTCAAC CAGGGTTGGC 120
CCAAGATAAA TATCTGATGT GTGGTTAGTC ATATGGTGAG TCAGTGTTCT AATCAGTGGT 180
AGAGTTAATC AGTCGGGGTT ACTCACCATG CCTAACTTTC ATGCACTCCT TCCAGAGGGA 240
AAATACATGC ATTCTTTTGG CATATTTGGT TTTGCATGTA CATCATTATG TTTCTCCTCC 300
CACTACCACA AGAAAAAGAT ATTAATTGTA GTAAAAAATA AAGTTATAAA CTTCTGGCAA 360
GCTAAAACTG AGAACAGGTT ATCAAAGGGA TGTGTGCCTG TTCACTTTTA GAAGTGTATT 420
AGGTCTTTCA TAGCTGAGAA AGGACAGAAA TAGGGAGATA AAGTCGTTCA CCTCAGATCA 480
CAAGCTAAAT TGGTGGTAAA GGCTGGACTA GAATCTAGAT GTAATGGGTA ACTTTCACCC 540
ACATTATGTC AGTCCCATTT AGACTTCCTT GGTTGACTAG TATTGATGTA ACCAAAAAGA 600
CATCTACTCA AAATTCAATA TTCTAATGGT AGTTATTGAG AACTTACTAT CTGTCTGGTC 660
CTGTTTAAAG AGTAGGACAT ATAGCAGTGA ATCAGGCACT TTTTTTTTTT TTTTATCAAG 720
AACTTTCTGG CAAAGATATA TATTTTGTTC CTGCGAGAGG CCATTTGTTG CATATCAACA 780
GCCAGATAAG CCTTAAACAA ACAGGTAATA AAAAGGACAG TCTTGGCTAC TCTTTTTGTG 840
ATTTAATCTA GAACAACATT TCTCTCTTGG TATTTACTTC ATCAGGCTGA TGTAAGGACT 900
TGCTACTGCA TTCATTGTCA GCAATGGTCA CAGCAGGCCT GAATACTTTT TTGTTGTTGT 960
TAACTGTATT TAAAGGTGTT GTACCATTCA CTTGCAAAGA AACTGTTTTT ATCAAATGAG 1020
ATTTTGCTTT GGAAGAATGG CAATGCAATT CAGCCATGTT TTTTTCTAAA TTAATGTAAC 1080
ATTTGCATAA TAATATTTTA AAGTAATTGC TTGGGCCACT TTCTTTTTTT ATTTTTTGCA 1140
GAAGAACTAG CAGATCGCTG TTAGAAAAAC ATTTGTTAAA TTTCCAAATC ATAATGTATT 1200
TTAGTGGTGA GAGGAGCTCA GTAAAGGAAA TTAAAGGCAT CGTGGACTCC ACAGAGCATG 1260
GAACACAATG AGCTCTCAAA AAGTCATTTG TTGGCAGATA TTGTTATTCT CATTTTACAG 1320
|
