| Tag | Content |
|---|
EnhancerAtlas ID | HS095-15993 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:28862020-28863790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr2:28863314-28863327 | GTAATGATGTCAT | + | 6.48 | | JUND(var.2) | MA0492.1 | chr2:28863313-28863328 | AGTAATGATGTCATG | + | 6.51 | | Rxra | MA0512.2 | chr2:28862981-28862995 | TGAACTTTCACCTC | - | 6.01 | | STAT3 | MA0144.2 | chr2:28862354-28862365 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_01568 | chr2:28861838-28863291 | Aorta | | SE_09812 | chr2:28862086-28863417 | CD14 | | SE_23318 | chr2:28861804-28864206 | Colon_Crypt_1 | | SE_26630 | chr2:28862555-28863347 | Esophagus | | SE_28044 | chr2:28862373-28863470 | Fetal_Intestine | | SE_31986 | chr2:28862564-28863350 | Gastric | | SE_35216 | chr2:28862226-28863847 | HeLa | | SE_50302 | chr2:28862021-28863860 | Sigmoid_Colon | | SE_52600 | chr2:28862061-28863547 | Small_Intestine | | SE_65622 | chr2:28861725-28865114 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I028639 | chr2 | 28862517 | 28863727 |
|
Enhancer Sequence | AGCCCTGGGC ATTCATTCCA GCTTTCAACT CCAGTGAGAG ATGAGAAGGA GAGTGTGGAG 60
GTAGATGGGA AATGAGAAAC AATGCTGTGT CCAGAGAGCT AAGAGAAGTC AGTGTTTCAA 120
GAGAGACAGA GCTGTCAACT TTGATGGATG CTTCTGAGAA GCCAAGCAAG TTGAAGACAA 180
AAAAAAAAAA AAATGATCTT TGGCTCTGCC CATATGGCGA TCGTTGGTGG CCAGGGCCAG 240
AGCTTCCATC CAGCGATGGA GACTGCAGAC TGGCTGGAGC GAGCAGCAGA GAGAAGGAGA 300
GATTAGGAAG TGCTGCCAGC ACCTATAGAC AGCTCTTCCC AGAAGTTATG AGAAGTAACA 360
GCCACGGTCA CTGGAGGGGA CATGGATCAA AGAAAGGGCA GGTGAAGGAG GGGAGATGTC 420
GGAGCAGGTT GTGTACTGAC GAGAAGGAAC CAGTAGAAAG GGAGAAACTG ATGCACTCAT 480
CAAACCCTTG TAATCACGAT CATCTTCTGT GTGAATTAGT TCTGGGTTCC TGGAATAGCA 540
TCGGGAATCA GCCGCGCTGA CCTTTAGCAT TTATTCTGTC ACTGTTACGA TAGACTTGAG 600
TTTCCTCAGT TCTTAAGAAA GTGGAAATAA TACTACCTTA TGTATGTAAG CCACCCCAAT 660
CACACGTGCT TTCATGCCAT CTTCTCATTT GATGCTCACA ACAAACCAAG GTGTCAGGAC 720
AGGATGTCAT GCCTGTCCCT AACCTCAGAG AAGTAGCCAG CCCAGCACTG CACAGCTCGT 780
TACCAGCAGA GCCTGGATCC CAGCCATCTG CCCATCGTGC TCAGTCTAGT CACCCTAGCA 840
TCTCTCCCAG GAACAGAACT GCCCTCCCTC CTCCAATTGT GTTACTAAGG AACGGGTGTA 900
AAAGGCCTTC AGACAACAGA AAGTGAGATC ATGGGCCAGG TGTGGTCATG AGCTCAGATA 960
GTGAACTTTC ACCTCCCTCC CTGGCAATAC CCTGTGGTCA GGAGCAGGCA GATTACACAA 1020
AGAGTGGAGG CTAGACGTTC CAAACAGACT CTGAATAGGT GACAGTGCCA GGGGCTCATT 1080
CTTCTCAGTG CTGGCCACAG GTTGGGCCTG GCTGCTGGCT AAAAGGTGCC GGGGAGGGGG 1140
ATACAGCAGC TCCCAGCTCA TCCTCAGAGG GTCCTGGGAT CAAAGGTATT TACACCCAGG 1200
GATATTTCAG ATAAATCTTT TCATCTATGT GGAAAACATA CAAAGTGGCG CAAGTGAGAA 1260
ACTCCGATTT CCTAAGGTTG ACAAGTCAAG TGCAGTAATG ATGTCATGGT AACCAATATG 1320
TTTCCAAACT TTCCTAAGGT TGACTAGCCC CATGCACTTT GAGAAGTTGG TAAATAGGAT 1380
TGTCGTCGTT TTATAAAATT GAAAACACGG TGTCTTGCAA TCACAGCCAC TCACAAAGGA 1440
AGCCAGAGAT GGTCCCAGCC CCTCCGCAGA CTTCCTGTGG ACTCAGGACT GGTGGTCTCT 1500
CCTGGGCCTT GCTGTACCCG GCAAATCCAG GGGCACAGAC TCAGGGTTCT GCCCTGCCGA 1560
CAGATGCTGC CTAGCCTTCT GTGTGTCATA AGTCAACTCC CGCTCAGCCC CAGGCTGCTG 1620
GGTCCCTGCT GTGGGCCAAA AACCAGCCAC TTCGCTGGTT TCTATCCCCC ACCCCGTTCC 1680
CGAGGGAGGG GCTCTGGTGT GAGACACCCC CTCAGAGAGG AAAGTGTCTC CCAGCTTTGG 1740
AGAGAATCGA GGTGTCCTTT CTCTCTCTCC 1770
|
