| Tag | Content |
|---|
EnhancerAtlas ID | HS098-41214 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:188066080-188068390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr3:188067159-188067170 | TTTCTGGGAAG | + | 6.02 | | Stat6 | MA0520.1 | chr3:188068359-188068374 | AGTTCTCAGGAAGCC | - | 6.68 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01557 | chr3:188066108-188066970 | Aorta | | SE_01557 | chr3:188067087-188068255 | Aorta | | SE_60963 | chr3:188056356-188170886 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I188347 | chr3 | 188065372 | 188068877 |
|
Enhancer Sequence | TGAGCCACCA CGCCCAGCTA ATTTTTTGTA TTTTTAGTAG AGACAAGGTT TCACCATGTT 60
GGCCAGGCTG GTCTCAAACT CCTGACCTCA GGTGATCCAC CTGCCTCAGC CTCCCAAATT 120
GCTGGGATTA CAGGCATGAG CCACCGTGCG TGGCTGAAAC CATACCCTTT TAACAGGACT 180
ATACCAGTGT ACTGTTCAAT ATACAGAAAT ACTATCACCC ATCTGATTAA TAATCCTTAT 240
CACAGCCCAA TGAGACAGGC ACAGATGTTC TGCTTTTCAA GATTCTATTT CCTAACTTCA 300
TCTTGACAGT TGTAAGTCTC TTGCTTCTCA AAGTTTGGTC TGAGGACCGG AAGCATCAGC 360
ATTACATGGG AGCTTGTTAG AAATGCAAAT CTCAGATCAT ACTCTAGAAC TTCTGAATGA 420
GAATCTCTAC TTTAACAAGA GCCCCAGGTA GTTCATATGC TCATTAGTGT TTGAGAAACA 480
TTCACTTCGG CCCTCGCCCT ATTTCAAGGC TATTGCTGTG GTGTGCTGAC AATGCCTGGC 540
ATGCTGCCAG CATTCTTGGG GCATGCTGTA CCATGCCTTG AGATAGCGGG GTCCGGGGGG 600
CGGGGATGCT GTGAAGTCAC TCCTTGGGAA TAATGGAAGA CTGGGTTGAA GGGATCCAGC 660
AGGCTTTATC TTTTTAACAC CCTTCATTTC CTTAGAAGTT ACTATTCAGA AGGGGTCAAA 720
CTGGGATTGG ATTCTAAGTC TTTCTGATCC AAAGTCCATG TTCTTTTCAT TAAACCACGA 780
TGTCTCAGTC AAGAGGAATG CTGGGTTGTG GGTGATAACT GTTCATTCCC TGTAGTGTGA 840
ATATTTCCAC ACTGGCTGCT TTACCCTATT ACTCAATTCC TAGAGGGGAA GAATTTTTTT 900
AAAAAAATTT AAAAAGCCTG AGTTGAAAGC CAGGATCCTG CAGCTTAATC AGTTATTTTT 960
GCTTTTTAAT GAGGGTGACT ATTGTGAAAT AAGTAATTAT TAATTACTCA AAACTAATGA 1020
AATATTTTAG TTTCCTTGCT CAAAAAGCAT ATGGATGCTA AAAGAAAGCA TATGGGTGCT 1080
TTCTGGGAAG CATATTGGTG AATGGACAAA TTACAGTGGT GCCAATATGC CTTTGCTGTC 1140
TGGCTGGGGC CATCAAAACG TGTGCTGGCA TCTGAGTCCT CGTGTGTTTA AAGGGATTTT 1200
TTAAAATTCC CATTTGATAA GTGCCTGGGG TTGCCTCTGG AGTTACACAG CGCTGTCTCA 1260
TCAATCTTTC TGCCATGCTT TCACTCAGAC ATTACTGGCT GAGTATAAAC TCGGTATAAA 1320
CCTTTGCTGT AAGTAGCTTC TGTGGCTCTT TCTTTCCAGA TGCCTCCTAT CCTCTGCAAT 1380
AGGTTCAGTG GGCCTGCCCC ATGGATGGCA CGTATGGAGA CTTTGTCTAT ACAACATTTT 1440
ACCACAGTGG TAAAAGCAGT AGCCGAAAAG GTGGCAGCAC TGAGACCTGT TTGCTCCATC 1500
AGGGACTCTG TCTGAGGCCC TCGGCCAGCT GTTGAATTGC TGCACTGCAA ATTTCTTACT 1560
TGTAAAACTG GAATGATAAT ACCAGTGCTC CTGAGCTCAC AAGCATGCTG TTCATCCAAT 1620
TTGCAGTCCA TGCCCTTTGC TCTTCCTCTC CTTTCCTTCA TGCCTCTTCT CCTTTGCTGC 1680
ACGTTCAGCT GGTCTAGTAA AAAGCTTGAT GGATTTGGAG GTGGCTGAAA CCATTTTGCT 1740
TGCTCTGGGG ATTGCACACT TCTGAGCTTG TCAGAGGCAG GCAACATGGC ATGTTTTAGA 1800
AGATACTTGG CTGAGTGTCC ACGAACTGTG GCTCTCAGAC CAACGTGACT TAGTAATCAT 1860
TTACTCAACA CCTACAAGCA AGGTAGCTTG CTAAGAAATT GAAGGAGGGA GCTGGCGGGT 1920
CTGTGGAGGT GAGTTTGATT CAGGGCCAGT CAAGACTTGG TGTGATGTGT GAGCTCAGTA 1980
ATTATACTTT GAGAGAGACA GAATTTGGAG AACTCTTTCC TATTGGAGGT TTCTTATAGA 2040
ACTAGGGACA AGAGCTGGCT TTGAAAGATT ATTAATTGGA CTTTGATAAG ATATTACAAG 2100
GATTTGAAGA GTAAGTCTCT GTCAGGCAAA AACCAGCTTG CAGTGGGACT CGGAAGCAGG 2160
CAAATATCAG GCATGGCTGA AGAACTGGGC ATCAATCACA GACATGTGTA GCTGAGAGAA 2220
ATCACTTCCT TTTGGTGAAC CCTAGACTCT ATCTGCAAAA TATGAGCTTT GAACAAGATA 2280
GTTCTCAGGA AGCCTCAAGA ACTCTAGCTG 2310
|
