Tag | Content |
---|
EnhancerAtlas ID | HS139-28126 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:26239990-26242120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr2:26241773-26241783 | CACATTCCAT | + | 6.02 |
|
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26240304-26241810 | CD14 | SE_26712 | chr2:26239870-26242089 | Esophagus | SE_28420 | chr2:26240306-26241937 | Fetal_Intestine | SE_29154 | chr2:26239992-26242119 | Fetal_Intestine_Large | SE_32014 | chr2:26240172-26241573 | Gastric | SE_35193 | chr2:26240079-26241982 | HeLa | SE_36382 | chr2:26240216-26241937 | HMEC | SE_64640 | chr2:26240168-26241940 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26240135 | 26241696 | chr2 | 26241064 | 26241266 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH02I026016 | chr2 | 26238975 | 26240088 | GH02I026017 | chr2 | 26240097 | 26242426 |
|
Enhancer Sequence | CCAGCCTTTT TTTAAAACAA GGTCTTACTC TGTCGCCTGG GCTGGAATGC AGTGGTATGA 60 TCTCAGCTCA CTGCAACCTC TGACTCCTGG GCTCAAGCAA TCCTCCCACC TCAGCCTCCT 120 GAGTAGCTGA GACTACATGC ATGCACCACT GCACCTGCCA TTTTTTCCGG ATTTATAGAG 180 AGAGGGTTTC GCCATGTTAC CCAAGCTGGT CTCAAACTCC TGGGCTCAAG CCATCCTCCG 240 GCCTCAGCAT CCCAAAGTAC TGGGATTATA GGCATGCACC ACTGCACCAG GCAAGGACAC 300 AGATTTTTAT TGTTCACCCA CAAAGTGCTT CACATGCACT ACTTTGTCTG ACCCTCACGA 360 CAACCTGCAA GGTAGGTATT GTATTCCTAC TGTACGGATG AGAAAAACTG AGACTCACAA 420 AGGTTAGTTA CTAGCTCAAG ATCATGTATG CCTCAGTGGC AGGGCCAGGA TTCAGAGCAG 480 GGTGGCCTGG AGGTCTGAGG TTGGAAGCAG GTGTCACCTT AATGACTTAG GAATGAGGTC 540 AGTGTCTGTG TCCTCCAATT ATGGTGCCAG GCTCAGTCTC TACGAATGCC TGGAGAATAT 600 GTCAGCACTT ACTGTAGCTT CATGTTTAGG CCAAGAAAAG GCTGAGATGA GATGATCCAT 660 GAGAGTTTTT CACAGAAACA CAGACCAAAC ACAGAAGCAA AATCTTGGTC TTCATATTGC 720 CCCAGACTTG TTCTCTTCTG GGACTGAACC TAGTGTTAGA ATCCTGCTCT GCAGGAATAG 780 GGGGGTGTCT TTACATTTCA TTCTGGTTAT TTGCCTAAAG CAAATCCCAG AGATACCCAG 840 AGAGGGAAGA CTTTCCTCTG CAGATGGTGG AAGATGCTGG CGCCCAGGCC ATCCTATGTC 900 ATCTGTATCC AGACACAGAT TCCAGATCCC TGTTCATGCC TCTGAGGACA TGGAGCGGGC 960 CTTTTAGCTC TCTTCAGAGC TAGAGTTTCA GGCATATGGT TGCTGCCCTG GATGACAAGG 1020 GTAGCACATG GGTGGGAACT CCAGATGCAT GTAAGGGAGC AAGAAGCTGC CCACTGAGGA 1080 GAATGCTGGG ATAGTGCAGG GCTGGGCTGG CCCAACTAGT TCAGCTCAGC CAGGAAAGGG 1140 CAGGTCAGAT CTGGCTCAGC AGGGGAGGCT GTGTCGGGGA GTGGTGCTGA CTCAGGGCCT 1200 GGTGAGTCAG GTGACAGCCA AGGACAGCTG TTGCCTGGGT GTTTTTAGAA AACTTTGGCT 1260 GCCAACCACT CTCTCATGGG TGCTTCTGCA CCTACTCAGA AGCAGGCAGA AAAAAGGAGG 1320 GCATCTTCTG TATAAGAAGC TCTGGGTGAG GGGTATTAAT ATCTGGCTCT ACTTATGTTG 1380 ATCCTTCCCA TGAAGTACCT AGAAAACGGA GCAGAAATTA ATTGAGAGGC TTCCAAATCC 1440 CTTCTGAATT CTCTGAAAAT CACTTATCTT TTCTGCTTAG CTCTTTTTAG GCACCTTGCC 1500 AGGTATCCAG CATAGAGGTT AAGAGAGCAG GCTCTGAAGT TAGGAGGGCC TGGGATCAAA 1560 ACCTAATTTC ATCATTTATA GTTGTATGAC TTAGATCAGA CTAAAAACAA CTTTTAATTA 1620 TGGAAAGCTT CAAATATATA TGAATGACAC ACATTAGTAT GATGAACCTC CATATACTCA 1680 TTATCCAGCT TGAATAATCA TTAACCCACT GTAACTTTAT TTCATCTATA CTCTACTTAT 1740 CCCCTTTGCT CCCACTTATT TTGAAGGAAA TACCAGGCAT CATCACATTC CATCTCTTTT 1800 TTTCTTTTTT TTTTGAGACG GAGTCTTGCT CTGTTGCCCA GGCTGGAGTG CAGTGGTGCA 1860 ATCTCAGCTC ACTGCAGCCT CCTCCTCTTG GGTTCAATGA TTCTCCTGCC TCAGCCTCCT 1920 GAGTAGCTGA GATTACAGGT GCCCGCCACC ATGCCTGGCT AATTTTTGTA TTTTTAGTAG 1980 AGATGGCGTT TCACCATATT GGCCAGGCTG GTCTCGAACT CCTGATGTCA GGTGATCCAC 2040 TCGCCTCAGC TTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTGCACC CCACCTTCCA 2100 TGTCTTTTCA CATCTTTTTC TTTTCTTTTC 2130
|