| Tag | Content |
|---|
EnhancerAtlas ID | HS098-13889 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:89774140-89776490 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:89774247-89774265 | CCCTGCTTCCTTCTCTCC | - | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr12:89774239-89774257 | CCCTCCTCCCCTGCTTCC | - | 6.22 | | ZNF263 | MA0528.1 | chr12:89774196-89774217 | CCCTTCTCCTCCTCCTCCTCC | - | 10.3 | | ZNF263 | MA0528.1 | chr12:89774193-89774214 | TCCCCCTTCTCCTCCTCCTCC | - | 10.66 | | ZNF263 | MA0528.1 | chr12:89774199-89774220 | TTCTCCTCCTCCTCCTCCTCC | - | 10.92 | | ZNF263 | MA0528.1 | chr12:89774208-89774229 | TCCTCCTCCTCCCTCTTCCCT | - | 6.09 | | ZNF263 | MA0528.1 | chr12:89774227-89774248 | CTCCTTCCCATTCCCTCCTCC | - | 6.21 | | ZNF263 | MA0528.1 | chr12:89774209-89774230 | CCTCCTCCTCCCTCTTCCCTC | - | 6.28 | | ZNF263 | MA0528.1 | chr12:89774181-89774202 | TCCCCTTCCCCCTCCCCCTTC | - | 6.29 | | ZNF263 | MA0528.1 | chr12:89774206-89774227 | CCTCCTCCTCCTCCCTCTTCC | - | 6.32 | | ZNF263 | MA0528.1 | chr12:89774172-89774193 | CTCTTCCTCTCCCCTTCCCCC | - | 6.3 | | ZNF263 | MA0528.1 | chr12:89774213-89774234 | CTCCTCCCTCTTCCCTCCTTC | - | 6.69 | | ZNF263 | MA0528.1 | chr12:89774230-89774251 | CTTCCCATTCCCTCCTCCCCT | - | 6 | | ZNF263 | MA0528.1 | chr12:89774242-89774263 | TCCTCCCCTGCTTCCTTCTCT | - | 6 | | ZNF263 | MA0528.1 | chr12:89774239-89774260 | CCCTCCTCCCCTGCTTCCTTC | - | 7.35 | | ZNF263 | MA0528.1 | chr12:89774184-89774205 | CCTTCCCCCTCCCCCTTCTCC | - | 8.16 | | ZNF263 | MA0528.1 | chr12:89774178-89774199 | CTCTCCCCTTCCCCCTCCCCC | - | 8.18 | | ZNF263 | MA0528.1 | chr12:89774187-89774208 | TCCCCCTCCCCCTTCTCCTCC | - | 9.51 | | ZNF263 | MA0528.1 | chr12:89774202-89774223 | TCCTCCTCCTCCTCCTCCCTC | - | 9.59 | | ZNF263 | MA0528.1 | chr12:89774190-89774211 | CCCTCCCCCTTCTCCTCCTCC | - | 9.98 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89773857-89774397 | Colon_Crypt_3 | | SE_27644 | chr12:89771389-89775687 | Fetal_Intestine | | SE_27644 | chr12:89776216-89781183 | Fetal_Intestine | | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | | SE_28566 | chr12:89776028-89781395 | Fetal_Intestine_Large | | SE_35767 | chr12:89772428-89774396 | HepG2 | | SE_35767 | chr12:89776061-89779121 | HepG2 | | SE_50215 | chr12:89772425-89774424 | Sigmoid_Colon |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I089382 | chr12 | 89776258 | 89780906 | | GH12I089368 | chr12 | 89761900 | 89775589 |
|
Enhancer Sequence | ACCAGGAGCC CTCCACCTGT TGAAATTATG TTCTCTTCCT CTCCCCTTCC CCCTCCCCCT 60
TCTCCTCCTC CTCCTCCTCC CTCTTCCCTC CTTCCCATTC CCTCCTCCCC TGCTTCCTTC 120
TCTCCCTTCT ACTTCTCGTC TTTTATTTAT TTGGTTTTGC TGCAGGTGCA ACTCCAGTAT 180
CCTGATGGGG GAAGCAACTT AAGTGTTTTT TTGTTTTTTT AAAACAGAAT CTCACTCTTG 240
TCCACCAGGC TGGGGTGCAG TGGCATGATC TGGGCTCACT GCAACCTCTG CCTCCTGGGT 300
TCAAGCGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCAC CCACCACCAT 360
GCCCAGCTAA TTTTTGTATC TTTAGTAGAG ACGGGATTTC ACCATGTTGG CCAGGCTGGT 420
CTCGAACTCC TGACCTCAGG TGATCCATCC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 480
GGTGTGAGTC ACTGTGCCTG GCCCAGTGTA TTCTTTTATT CAACAACATT TGTTGAGTAT 540
CCTGGACCAG GTACTGGTAA ACTAGATAGG CAACGTCCTT GCCTTGGAGG AGCTTCTATT 600
CCAATGGAGG GAGACAGAAG CCAATGATGA TTTCAGATCT GCTTGGCCCA CAGGGAGCCC 660
CTGGGTCTAA CATATGGGCA GGGGATTCCA AAGTCCTTAC TTTCCAGGTG GAAATGGTTG 720
CTTGTATGAA GTAGCAATTA GATGAACACT TCAGACAAGG ACAATCAAAA CAGGAAGTTG 780
TCGATTTCAA ATACCTTCAA AGAAGGAAAA TGTTTCAGGG AAGCTTTTAC TTCCATGGAC 840
TTATTTCAGC AGTTCTTTGG TCTTATGTGA GACCTTTTAA TGAGTCCCTT GCATTTATGA 900
AATGCTGTAT GACTGCACAC AGTCCCTTCG TGCATGTGAC TTCACTTGGT CCTGTGAGAA 960
GGACTGAGCA GGTATTATCC TGATTTTACA AATGAGAAAA CTGAGGCTCA AACAACTTGC 1020
CCAAATGCAC CCAGCTAGCT TAGGTGTATG ACTAGAAACC AGGCTTTCCC CTTTCCTGAT 1080
CAACACCACG AACCTCACTT CTCTCTTGCC TCCCTCATGG TCATCTTTTT CATCCATCAC 1140
GAAGGGCGCT GCTGCTGTGG GTTTGACTGG GATTACCCAT GATATTTTAG GAATATGATA 1200
TTCTGGGAAA GAGGACATAC CCCCCAACAT ACACACACTC CTAAAAAGTA TATATCCCTG 1260
TAATTTGCTA CCATCATTTG TCAAAAATTA TTAGCTTCAA GCCTTTATGG GGGCCCTGGC 1320
TCAGAGACCA TTCAGGAAAA GAACCAAATT TCCAGTGGCA TCTATCTGTT CTAATGCCAG 1380
CACTGTGGTC ATAGGAAGCC ATCCACAGAG GATACAACAT ACCTAATTAT TATTTGGCAT 1440
CAAAAACACC AGGAGCAGGA ATATTGATGA CATATTAACA GTGACTTCTG AATGTATAAC 1500
CATATTTGCC TGATTCATCC ATCCCTATAA AAATTGATCA AGCTGGGCGC AGTGGCTCAT 1560
ACCTGTAATC CCAGCACTTT GGGAGGCTGA GGCTGGAGGA TCAGCATAAG CCCAGGAGTT 1620
TAAGACCAGC CCAGACAGCA CAGTGAGACC TCATATTTAC AAAACTTAAA AAAAAATAGC 1680
TTGATATTTT GGCATATGTC TATAATCTCA GCTACTAGGG AGGCTGAGGC AGGAGGATTG 1740
CTTGAGCCCA AGAGGTTGAG GCTGCAGCAA GCTATAATCA TGCCACTGCA CTCCAGCCTT 1800
GGCAACAGAG CAAGATGCTC TCTCTCTCTC TCTCTCTTTT TTAAATGATC AGTTTAGTGA 1860
TAACAGAGTG GAAACCACAT ATAAATAAAC TTTATTACAA TAATGTGTCC TCTACTAATG 1920
AAAGTTAAGA TTTATCTAAC ATCTCTTATG AACCAGCCCC TATGCTAAGT GTTTCATGTA 1980
ATTATCTCAT ATAATCTTTA CCACAGCCTT TTAAGTTAGG TGCTGTTATT ATAACCATTT 2040
TACAGATGAG GAAATTGAGG CTCCGAAAGG TAAACTGTTT TGCCCAACAA TATATAGCTA 2100
CATGGTGATA GAACTAGTGT TTGAAAGTTG GGCGGTCCGA CTGTAAAATC TCTTTCCTAA 2160
TCACTGTTCT AATTGGTGCA CAGATTATTA GAGTTAGACC TTAGTTGAAC TTCCTATTTT 2220
AGACAGATGG AAGCAGAGGC CCTAGCAGAT TAAGGATCTG CTTAACGTCT TCACCAACAG 2280
AATGAGACTT GCTTCTACAT TGCCTCTCAA CTGGAGAAGA GCTGGAATGA GTCTTTTGAT 2340
TTTCGCCTAT 2350
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