| Tag | Content |
|---|
EnhancerAtlas ID | HS118-11098 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:239214000-239216260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr2:239215158-239215170 | TCTATTTTTAGG | - | 6.14 | | REST | MA0138.2 | chr2:239214175-239214196 | GCCGCTGTCCATGGGTCTGAA | - | 7.68 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23101 | chr2:239213754-239214413 | Colon_Crypt_1 | | SE_23101 | chr2:239214748-239215698 | Colon_Crypt_1 | | SE_23739 | chr2:239214902-239215671 | Colon_Crypt_2 | | SE_24713 | chr2:239215040-239215630 | Colon_Crypt_3 | | SE_52761 | chr2:239214668-239215660 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I238305 | chr2 | 239213755 | 239214413 | | GH02I238306 | chr2 | 239214669 | 239215698 |
|
Enhancer Sequence | GGCTGCTGGG TGCCTTTTCC ATGGTGGTGC TCTCTGGTGG CTGTTAGCAG GGATACAGAG 60
ACCTTCACAT GCCTGTCCAC TCCCATGGTC CTAGCTGCAT GCATGACCCT TCCACTAAAC 120
TCCTGGTCCC CAACCTTTGA ATTTTCCAGG CCCAGAGCAG CAACAGCCGT CTTTTGCCGC 180
TGTCCATGGG TCTGAACATA TTCTTATGCC AAGCCACTTC TCTTTCTACA CAAAATGGAG 240
AGCTACGTGT ACTGCCTAAG CATGGTGGGC AGAACGGTGG GCCCCCACAC ACGCCCATGT 300
CTGGAACCTG TACATCTGTT TTGGTACAGG GTAAAAGGGA CTTTGCAGAT GTCATTACAT 360
TGAGGATCTT GAGATGGGAA CATTATCCTG GATTATCTGG GTGGCCCAAT GTAATCATAA 420
ATGTCCTTAT AAGTGAAAGA GGGAGGCCGG GTGTGGTGGC TCACGCCTGT AACCCTAGCA 480
CTTTCAGAGG CTGAGGCGGG TGGATCACCT GAGGTCAGGA GTTCGAGACC AGCCTGACCA 540
ACATGGTGAA ACCCTCTCTC TACTAAAAAT ACAAAAAAAA TTAGCTGGGC CTGGTGGCGG 600
GCACCTGTAA TCCCAGCTGC TCGGGAGGCT GAGGCAAGAG AATCACTTGA ACCCAGGAGG 660
TGGAGGTTGC AGTGAGCCAA GATCGCACAA TCGCACTCCA GCCTGGGCAA CAGAGCGAAA 720
TTCCATCTCA AAAAAAAAAA AAAAAAAAAA AGTGGAAGAG GGAGCCAGGA GGGCCAAAGT 780
CCGAGAAGAA GGCGTGGCCA TAGAAACAGA CGTTAAAATG ATGTCGTTTC TGGAAAGGGT 840
GCATGAGCCA GAGAATGCAG GTAGCTTCTA GAAGCTGAAA AAGGAGAAGA AATGGATTCT 900
CCCCTAGAGC CTCCAGAAGG ATTACAGCCC TGACCACACC TTGACTTCAG CCCAGTAACA 960
CCCAGTTTCA GCTCTGACCT CCAGAATTGT AAGAGATTCC ATTTGTGTTG TTTTAAACTC 1020
CCAAGTTTTT GGAAATTGGT TACAGCAGCA ACAATGAACT AATACACCAA GTTTCTGTCC 1080
ATGGGGAGAT TGGGAGAGGC AGTCTGTCAG CACTGCCTTT CAGGGAGGCC CCGGAGTGAG 1140
GCTGCAGTGC AGCAGCTATC TATTTTTAGG CATTTTTTGC ATCCCACACT GAGCCAACCC 1200
ATGCATGAAC CAAGCTCGGC CTATTTCTTC CTCCACTAGG TGGTCATAAG TGACACCGCC 1260
ACCCAACACA GCAGTGATGA AGGTGAGGGA CCTCCAGTGG TGCAACAGAG GCAGATGATA 1320
GGAGGGTCTT GTGCAGTTTA TCTGTGGCTC TGGCCCTGCA TAAGCCCAGT GCTGGATGTG 1380
CCCTTTCATC TTATCATAGA TTTCTGTCGA GCATGCCTGA CCTATGCCCT GGAGGCCCTG 1440
GCAGAGCCCG GCTCAAGGCA GGCAGCTCTA GTGGTGTGAT CACCGCTTGG TGTCTTCCGC 1500
TCTGCTAGGG TGCAGAGGCA TACCAGCATC TGTCTTCCTT TGCTGCAGAT AGCGTGGCCT 1560
TACTCCAGAA CCCCCAGGGT CCAGGTTGTG ATTCTCCCAC TGGGGGTTTG CCATGAAGTT 1620
ATCACACACT CAGAGATTTA AAGCAACAAG GCATCTTTTC CACCATAGGT ATCTCTAGAA 1680
CCATAGCATC TTCCAGATCA TTTGGCCTAA TTTGCTGGAT TGCTAGCACC ATAGCCTGTG 1740
CCCACTGCAG CGTTCTTCCC CATGCTGGCA GCCTTTCACA CCACCTGGTA AATGTGACCA 1800
CGCAGTATTC CCAAGTGTGG CACGTGCTGC CTCCAGAACC CACAGAGGCG ACCAGTCCTC 1860
GTGGTCCTTC TTAGTGGTGG GAAGTACACA ATGTAGTCCT TCCTTCACTG TGGAGATGCC 1920
TGTTAAGCTC CAACCACTGG GCCCCTAAAA ACTTCACCGA TGCAGCAGAC GCCTGGAACT 1980
TCACAGGGTT TCTCTCCCAC CCTCTGCAGC ACACGCACCT TAATAAGGCC TCTGAGGTTT 2040
CTCCTCGTCA ATCTGGTCAT CCAGTTTAAT TAATAGGATA TCAGTATACT GAACCAGTGC 2100
AGCATTGTGC AGAGTGTCTG GTCCATCCAG ACTATATTAG GAAAGAGGGA AAAGAGTTAA 2160
TATGGCCCTG GGGTGAGACA ATCAGTGTGT ATTCTTCTTC TTCTTCTTCT TTTTTGTTTT 2220
CTTAAGACGG AGTCTCAATC TGTTGCCCAG GCTGGAGTGC 2260
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