| Tag | Content |
|---|
EnhancerAtlas ID | HS095-28143 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:76638620-76640850 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr7:76639672-76639687 | AGATGACTCAGCAGG | + | 6.66 | | Nr2f6(var.2) | MA0728.1 | chr7:76640759-76640774 | GAGGTCAGGAGTTCA | + | 6.22 | | TCF7L2 | MA0523.1 | chr7:76639689-76639703 | AAACATCAAAGGAA | + | 8.12 | | Zfx | MA0146.2 | chr7:76640735-76640749 | GAGGCCGAGGCGGG | - | 6.01 | | Znf423 | MA0116.1 | chr7:76638680-76638695 | GGCACCCATGGTGGC | + | 6.18 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26739 | chr7:76638557-76640122 | Esophagus | | SE_68923 | chr7:76639200-76640242 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I077009 | chr7 | 76639119 | 76640130 |
|
Enhancer Sequence | GAGAGGAGGA GAGAGAGCTA CTCAGAGAGA CCAGGGGTGT ATACGGTCCT GTTCTGCAGT 60
GGCACCCATG GTGGCCAAGG GGTGGTAGCA GGGATTGTGG GCTGGGAAGA ACCAGATCTG 120
AACCAGGGCA GACACAGAGG ATTGGAGAGG AAGAGTTGGA TTCCAGAAAT ATGCAGGAGG 180
TGGCCGCAGG AATTGGGAGA TAAGGCAGAG GGAAGAGGCC ATGCCCAGTT TCTGATGTGG 240
CCTGGGCGTG AATGCAAAAA TTGGGGTCTT CTGTGCTTTG CAAGTGAGTG CACCACCACA 300
GTTTGCTTTA CGGCAAGGCC CCAGGAAAAG GGGTTCTGGG GATGTCATCT CAACGGCAGG 360
TGTGTTCCAC AAGAACATTA ATACATCGTT AATATTTTTG AAAGACAAGA CTGGGCATGG 420
TGGCTCACAC CTGTAATCCC AGCCCTTTGG GTGGCTGAGG CAAGTGGATC ACTTGAGCTC 480
AGGAGTTTGA GACCAGCCTG GGCACCATGG CAAAACCCCG TGTCTACTAA AAATACAAAA 540
AATAGCCAGA TGCGGTGGCT CGTGCCTGTA GTCCCAGCTA CTCGGGAGGC TGAGGCAGGA 600
GAATCGCTTG AATCTGGGAG GCAGAAGTTG TAGTGAGCCG AGATCACACC ACTGCACTCC 660
AGCCTGGGCA ACACAGCGAG ACTCCATCTG AAGATAAAAA AAAAAAAAAA AGAAGAACCC 720
AAGGGAGGGG GCACTGCCCA GCACAGGCAC AGTCCCATCA GGCCCTGGGG AGCCATGCCA 780
GGGCGTTCTG CCCAGCACAG TCACACCTAA AAGGGTCCTC AGCCGAACCC CATCCCCTTG 840
AATACCAGCT CATGACGGCT TTGAGCAGAA CATGTCACGG GAACGGCATT GTGTAGAACT 900
TTTTATTAAA TGGCATTTAA AATATTCCCC AGGACTGTGT AGCTGGGGAA ACACCACAAA 960
ATCCATTGGC CCGGAACATA ATGGCTCAAT GGTACGAAAC AAATGCATTG TTAAAAAGGA 1020
AAAACAGCAA CTGTTGCGGG GTAATGACTT GCAGATGACT CAGCAGGCCA AACATCAAAG 1080
GAATTCGGAT GGCAGCAGGT GGGCACAGGC AGCCAGGAAG CACCCCTCCC TCGCTCTCAC 1140
TTCCAGCGAT CGCTTTACCT CCCTGGAGTG TCTAAGCCAC CCATTTCTCT CCATCATCCC 1200
TGCAATCCCC AAGCAAGAAC CACCTTGGTC TCCCGCTGGG ATGTCCGTGG TTCCTCTCTA 1260
GCTGAACTCT CCATGTCCAC TCCTGCCCGT CGCCCATTCC CCTCTCAGTA TCCAGAGGGA 1320
CCAGGTTCTT TGTTCTTTTT TTTTTTTTTT TTTTAAGATA GAGTCTCACT CTGTTGCCTA 1380
GGCTGGAGTG CAGTGGTGTG ATCTCGGCTC ACTGCAACCT GCAGCTTCAG GTTCAAACGA 1440
TTCTCCTGCC TCAGCCTCCC AGGTAGCTGA GACTATAAAC GTGCGCCACC GTGCCTGGCT 1500
AATTTTTTTG TATTTTTAGT AGACGGGGTT TCACCATGTT GACCAGGCTG GTCTCAAACT 1560
CCTGACCTCA GGTGATCCAC CCACCTCGGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG 1620
CCACTGCACC CAGCCAGGAC CAGGTTCTAA ACCTGATCAC ATCACACCTC TGCTCCCAAC 1680
ATTCAGGAAC TTCACACTGC AAGAACAGAA TCTAGGTTCA GACAGGTGTG GCGGCTCACA 1740
TCTGCAATCC CAGCACTTTG GGAGGCCAAG GCAGGCGGAT CACTTGAGGC CAGGAGTTCG 1800
AGACCAGCCT GGCCAGCATG GTGAAATGCC ATCTCTACTA AAAATACAAA AATTAGCCAG 1860
GCATGGTGAT GGGCGCCTGT AATTTCAGCT ACTTGGGAGG CTGAGGCAGG AGAATTGCTT 1920
GAACCTGGGA GGCGGAGGTT GCAGTGAGCT GAGATCACAC CACTGCACTC CAGCCTGGAC 1980
GACAGAGCGA GGCTCTGTCT CAAAAAAAGC AAAACAAAAT AAAACATACC AACATCTAAT 2040
CTCTATAAAA TATTTTTAGA AGTTATCCAG GTGGGCCGGG TGCAGTGGCT CATGCCTGTA 2100
ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG AGGTCAGGAG TTCAAGACCA 2160
GCCTGGCCGA CGTGGTGAAA CCCCATCTCT ACTAAAAAAA AAATACAAAA ATTAGCCGAT 2220
TACAGGCATG 2230
|
