| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29466 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:239182480-239184380 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:239182527-239182542 | CGATCTCTTGACCTC | - | 6 | | TBX20 | MA0689.1 | chr2:239183898-239183909 | GAGGTGTGAAG | + | 6.02 | | Zfx | MA0146.2 | chr2:239182550-239182564 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_23101 | chr2:239182614-239184068 | Colon_Crypt_1 | | SE_23739 | chr2:239182564-239183631 | Colon_Crypt_2 | | SE_24713 | chr2:239182517-239183795 | Colon_Crypt_3 | | SE_28235 | chr2:239182299-239184516 | Fetal_Intestine | | SE_29205 | chr2:239182289-239184636 | Fetal_Intestine_Large | | SE_50608 | chr2:239182511-239183864 | Sigmoid_Colon | | SE_52761 | chr2:239182384-239183906 | Small_Intestine | | SE_65405 | chr2:239182095-239183795 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I238273 | chr2 | 239182267 | 239184529 |
|
Enhancer Sequence | GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG ATGGTCTCGA TCTCTTGACC 60
TCATGATCTG CCCGCCTCGG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGCGC 120
CCGGCCCCTA GAAAGTCTTT AATCATGATG GTATATTCAC TTTTCCACAC AGGACCACAT 180
GGCAACCCCT GCACATCTGA CTCCCTGGGT GATGCCATCA GACACCCCCA TCCAGGCAGA 240
ACTGACTGCT TAAAAAAATA ACAGGCACAA GAAACATTTG AAAGAAAGTT TTCAAAATAG 300
AATCTGAAGA GGAGGGCCAC TCCATCTGAG TTCCCACGTC ATCCTGGGTG TATCCGGCGG 360
GCTCTGGGGT GACAAGCCTG TCTCTGGGTG TCGGTGCTCA TGGCCACAGC GGCCCTCACT 420
CCAGGCGGGA GCAAAGGGGC CAGCTCGAGG CTGCCACTTG CCCTCAGGGC TCAACAGGCC 480
CCGGACACAT GAAACCTGGG GCTGCGTTAC GAGTCTGACC CAGGATTCTG CCACGCGTGT 540
GCTTCCTGCA ATGTGGTGAG GAGACCTTTG GACCCACAGC TGGGTCTCAT ATGCTTTCAG 600
TTTTGCCACC TTCAGTAATT TCAGAAACAG GCACATTTCT GAGTATGCTC TGAAATCAAG 660
ATATAAACTG CTGGAAAGTG TGGAAAATGT CCATGTGGCA GAGCTTCTGA GCTGTGAAGT 720
TACTGTAGAG GCCAACAGGG AAACACCTTA AATGGACATA ATCACTGGAG AACAGAGCAG 780
CCCAACTGAT CAGAACGAAC TTTCCCTTTG GCTCCTCCTT CCGGAAAAGG GGGCCTCCAC 840
AGGCACGCAG GCCCAGAGCG GTGCCCTCCA TGGTGGGGTG CTCATCCCAG GGGCACCGGA 900
TTTCCATGCG GTATCTTTAG ACCTGACCAG CACCGACGAG TAGCCCAGGC ACCTTGTTCT 960
GTCTGTATCA ACCCTCACAA AATGGACAGT GGGATTAGGG AGGAGCCTGC AGAGAAACTT 1020
AGAGGACACC CAAAGCCAAC ACCCAAAAAT GCAAGAGTCC AAGCTAGCAC ATGGCAGAGC 1080
AACCCTTCCA CACCTGGCTC AAGGGACCCC AGAGATGAGT GCTGATGACC TGCTCACTGC 1140
TGATGAAAAA CTACCCAAAC ATTTAAAAAT ATGAAGACTG CTTCAAATAC GAGTTTATAC 1200
CCATGATTAC TAGTGAAGAA CTTTGCCCTA ACTGTACACT GTGCTTTGAA ACGACTGATA 1260
ATAGAATACA GCTACTGCTT CACCTTTAAG CCTCTCAGAT TTTTCTATTT TTATGCATGT 1320
TTTTAATGTA CAAGATCCAC CAGCCCCTTA GTGCATGTGC GCAACACATG AAAAGGCACA 1380
GCTCCACAGT CGGGAGGTGC TCACACACCA ACTGGCAGGA GGTGTGAAGA TGCTCTGCAG 1440
GGCACCTTCC TTTCCCACCC TGGCTGACAC TGATGGTCTC TGCCTGCTCG TCACAACAGA 1500
CCAACACAGC TAAGGAATTC TTCAAAGTTC TGGAGGTGGT AGTTTCCACT CTAAAGAAAA 1560
AAGGCCAGGC CAGGCACAGT GGCTCACACC TATAATCCCA GAACTTTGGG AGGCTGAAGT 1620
GGGAGGACTG CTTGGGTCCA GGAGTTCGAG ACCAGCCTGG GCAACATAGT GAGACCCCAT 1680
CTCTACAAAA AATACAAGAA TTAGCTGGGC GTGGTGGTAC ACGTCTGTGG TCCCAGCTAC 1740
TCAGGAGGCT GTGGCAGCGG AATCGCTTAA GCCCAGAAGT CAAGGCTGCA GTGAGCTGCG 1800
ATGAGCCTCG AGTTTTAGAA AGTCAACACA ATCCAAGCTA TAATTTGGGG GGATTTAAAA 1860
CATATTTCTA TAGGTTTGGA GCAGATGTGC GAGGCCGACG 1900
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