Tag | Content |
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EnhancerAtlas ID | HS037-32409 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr6:6686720-6688200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr6:6687267-6687278 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr6:6687214-6687224 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr6:6687267-6687277 | GCCCCGCCCC | + | 6.02 | NFAT5 | MA0606.1 | chr6:6687742-6687752 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr6:6687742-6687752 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr6:6687742-6687752 | ATTTTCCATT | + | 6.02 | SP1 | MA0079.4 | chr6:6687336-6687351 | GAAGCCCCGCCCACT | + | 6.79 | SP1 | MA0079.4 | chr6:6687409-6687424 | GAAGCCCCGCCCACT | + | 6.79 | SP2 | MA0516.2 | chr6:6687335-6687352 | GGAAGCCCCGCCCACTC | + | 7.16 | SP2 | MA0516.2 | chr6:6687408-6687425 | GGAAGCCCCGCCCACTC | + | 7.16 | SP4 | MA0685.1 | chr6:6687336-6687353 | GAAGCCCCGCCCACTCC | + | 7.17 | SP4 | MA0685.1 | chr6:6687409-6687426 | GAAGCCCCGCCCACTCC | + | 7.17 | Sox6 | MA0515.1 | chr6:6687891-6687901 | CCATTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr6:6688034-6688055 | CCCCCTCTCCCTCCTTCCTTT | - | 6.09 | ZNF263 | MA0528.1 | chr6:6688033-6688054 | CCCCCCTCTCCCTCCTTCCTT | - | 6.23 | ZNF263 | MA0528.1 | chr6:6687222-6687243 | CCTTCCTGGGCCTCCTCCTCC | - | 6.26 | ZNF263 | MA0528.1 | chr6:6688030-6688051 | TTGCCCCCCTCTCCCTCCTTC | - | 6.53 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_09354 | chr6:6683600-6691412 | CD14 | SE_23153 | chr6:6686849-6687239 | Colon_Crypt_1 | SE_23153 | chr6:6687440-6688256 | Colon_Crypt_1 | SE_23777 | chr6:6686868-6687273 | Colon_Crypt_2 | SE_23777 | chr6:6687443-6688192 | Colon_Crypt_2 | SE_25016 | chr6:6686522-6688268 | Colon_Crypt_3 | SE_26283 | chr6:6686087-6691556 | Duodenum_Smooth_Muscle | SE_26869 | chr6:6686831-6691114 | Esophagus | SE_27854 | chr6:6686469-6688323 | Fetal_Intestine | SE_28835 | chr6:6683151-6688228 | Fetal_Intestine_Large | SE_29666 | chr6:6685835-6691263 | Fetal_Muscle | SE_32005 | chr6:6686469-6688437 | Gastric | SE_33501 | chr6:6686421-6690127 | H2171 | SE_34700 | chr6:6685359-6691754 | HeLa | SE_42348 | chr6:6686682-6692616 | Lung | SE_48756 | chr6:6686740-6688299 | Right_Atrium | SE_50192 | chr6:6686878-6691045 | Sigmoid_Colon | SE_52541 | chr6:6686153-6688359 | Small_Intestine | SE_65078 | chr6:6686516-6691258 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I006683 | chr6 | 6683386 | 6691167 |
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Enhancer Sequence | TTGGATTAGA GCCCATTCTA ATGCCTTCGT TTTACCTTAA TTATCTTTTT AAAGGCCTCA 60 TCTCCAAATA CAGTCCCAGT CTGAGGTATG AGGAGGTTAG GGCTTCAAAT ATGAATTTTG 120 AGGGACACAT TTCAGATTAT AACAGATACA TACATATGTA TATCCTATAA ATGAAAATGT 180 CAGGACGGAT TTTAGAGATA CAAGTTTTTA CTTAATTATG ATCCCCCAGC GATCTCATCT 240 CCTCTTAGTC TCAATTTTTC TTGTCTAAGA GAGGGTGCTC CTACCCACAT CTTCAGTCCA 300 AATCCCTCTC CTGAAGGTCG GACCCGCATT TGCAGTGACG GTGACTGGAC ATTTTCTCCC 360 AGGTGTTCGT CAACACTTTC AGCCCTACAG GTCTGAAACA AAACTTACCC ACCTCCAGTG 420 AAGCTCGTCC TCCTGGCCTT TCTGCTTCCT TTTTAAAGTC CATCCCCCTC CAGGCCTCCC 480 ATTACCGGCT GGGAGCCCCG CCCCTTCCTG GGCCTCCTCC TCCGGGGCTT TCAGCTCCTG 540 GCTGGGAGCC CCGCCCCCTC CAGTCCGCCT TTCCAGGCTG AGAGCCCCGC CCATTCCAGG 600 CCTCATCTCC TGGCTGGAAG CCCCGCCCAC TCCAGTCCTC ACCCTCCAGG CTGAGAGCCC 660 CGCCCATTCC AGGCCTCATC TCCTGGCTGG AAGCCCCGCC CACTCCAGTC CTCACCCTCC 720 TGGCTGGGAG CCCCGCCCAC TCCAGGCCTC ACCCTCCAGG CTGGAAGACC CGCCCCTCCC 780 GGGCCTCCGG ATCCTGGCTG GGAGCCATCT CTGCCTCCTG CCGCTTCCTG CACTCCTGAT 840 CAGGTCAGTG GCCAGTCACA GACCTCTGAA ATGTCCTTCC TGACTGTTAG CTCCACAGCA 900 TTCCTACAGC TCCCGCCGCA GTTCCGCCCT CCGGAGGGTT CCAACAGCAG CCCAGTGCGC 960 CTCCCCAGCC CCAGGCTCCC TCCACTCCAG TGAGCCTGCA CCTGGCGCTC CCTGGCACAC 1020 ATATTTTCCA TTGCTCTTCA CTGCCAATTA AATGCAAATT TCTCATCGTG GGGTTCCAAG 1080 TTCTCTGTAT TTGGTCCTCT TATCCTGACA GCTCTACCCT CCCCAGAGCA CTACAATCTG 1140 GCCAAGAGCC TCACCAGCCT ATTCCCCCGA ACCATTGTTT TATTTATTTT AGATTCAGGG 1200 GTATTTGTAT GCAGGTTTGT TACATAAGTA TATTGCGTTA TGATAAGGTT TGTGCTTCTG 1260 ATGATGATCC AGTCGCCCAA CATAGTACCG GATAGTTAGG TTTTCTTCCA TTGCCCCCCT 1320 CTCCCTCCTT CCTTTTGGGG TCCCTGGTGT CTGTTATTCC CATGTTTATG TCCTTATGTA 1380 CCCAGTGTTT AGATCCCACT TATAAGTGAG AGCATGTGGC ATTTGGTTTT CTGTTTCTGC 1440 ATTAGTTTGC TTAGAATAAC GACTGCCAGC TGCATCCATG 1480
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