| Tag | Content |
|---|
EnhancerAtlas ID | HS104-55455 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr7:99374080-99375650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr7:99374469-99374484 | AAACTAAAAATAAAA | + | 6.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29221 | chr7:99374271-99377397 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I099776 | chr7 | 99374272 | 99377397 |
|
Enhancer Sequence | CAGACTGGAT AAAGAAAATG TGCCACGTAT ACCCCATGGA ATACTATGCA GCCATAAAAA 60
AACAATGAGT TCATGTCCTT TGCAGGGACA AGGATGAAGC TGGAAACCAT CATTCTCAGC 120
AAACTATCAC AAGATCAGAA AACTCAACAC CACATGTTCT CACTCCTAAG TAGGAGTTGA 180
ACAATGAGAA CACATGGACA CGGGGAGGGA AACATCACAC ACTGGGGCCT GTTGTTGGGT 240
GGGGGGCTAG GGGAGAGATA GCATTAGGAG AAATACCTAA TGTAGGTGAC AGGTTGATGG 300
GTGCAGCAAA CCACCATGGC ACGTGTATAC CTATGTAACA AAACTACACA TTCTATGCAT 360
GTAACCCAGA ACTTAAAGTA TAATTTAAAA AACTAAAAAT AAAAAATAAA ATAAAATCAC 420
AGTCCATCAG CCCGCCAGTG GTTAAGAATA TTCAGCATTT CTTCAAATTC AGCAGGAAGG 480
TATAGACAAA GAAATGCTTA TATACCCTTC TATTAAAAAG TCTTGGCTTA AATTTAATAA 540
CAAAACAGAA TGAAAAGTTC CACACTTGCA GATAAAATTA AAAAACAACA ACAGCAGAGT 600
ATAAATGGTT TGCCAATCTA TTTCTCTATT ATCTCTCAAC CCTTCATTCA AAAGCACTTT 660
AAATCCAAAG TCTAAATGAA AGAGTTTTGG CTTTTAATTG AAAGTGAATT GATGTGGGAA 720
GGAGATGATA TGATGTATTT ATGAGCACAT ATTAGAAGGG TCTGAGACAA CACATGTAAT 780
AAAAGGGCAC CTAAGGAAAA AAAAAAAGAA GAGGGGAATA GGCAGACACT GGACAGAGCA 840
TGATGCTGTG AGTCCCTGGG CCACCAAAGT CTGGAGAAAA GTAATCACAA TGCTCCCAGC 900
CTAGTTCAGA CTGTAGAACT TGACACCTGG TGACACATGG GATCCTTGGT AGGACAACCT 960
TCGAAAAGTT TTACAATAAC CAGTGTGAAT GTTGTTAGAA CCAAAATGAT GTCACTAGTT 1020
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTAAAAACCC TGACAAATAA 1080
ATCAAAGAAG GCTATGAAGA GAGGATTCTC ATGCTTGTGT GCCTGATAAC AAAACTATCA 1140
CAAAAGACTC CGCAAAACTA CAAGCTTGCA CAAAGGCCAT CCCAACATTA AAAAAAATAT 1200
TTCTGCAAGG ACACCTGCCC AGCAACTGCC TGTCCAACCT TGGTGAGGCG TCACCCTTGT 1260
TACTGATCTT TGTAGCGAAG GATAATTATT TCAAAACTGA TAAGAAATCC TCCTCATATT 1320
TTCCTTGGAG CCTCTTTGTC TTGCTTTACT TCCCTGAATT TGCACATAGT TTATAAAGGC 1380
ATGCAGATTC CCATTGCAAT ACTCTACACC CAAATAAATA TCTTCTTCTT TCAGAGAACT 1440
TCTCTCTGTT TGTAGTTAGG TTGACAAGAG CTTCATCCCA AGAGGCTTTG GGCTGAGACT 1500
GTCCTCTGTG CAGTGGGGTA AACTCATCAT AGAAACAAGT CTATCCAATG GAAGTTTCCA 1560
GAATACTCAC 1570
|
