| Tag | Content |
|---|
EnhancerAtlas ID | HS045-31439 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr19:6065420-6068090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr19:6066005-6066016 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr19:6066006-6066016 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr19:6066003-6066020 | CTGGGGGCGGGGCTGGG | - | 6.03 | | ZNF263 | MA0528.1 | chr19:6066122-6066143 | GGAGGAGGTGGGGGAGTGAGG | + | 6.81 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00353 | chr19:6065551-6068885 | Adipose_Nuclei | | SE_01604 | chr19:6065279-6066959 | Aorta | | SE_01604 | chr19:6067055-6071713 | Aorta | | SE_09597 | chr19:6059621-6068905 | CD14 | | SE_12907 | chr19:6064951-6068518 | CD34_Primary_RO01480 | | SE_13400 | chr19:6064969-6068546 | CD34_Primary_RO01536 | | SE_14082 | chr19:6064531-6068692 | CD34_Primary_RO01549 | | SE_23458 | chr19:6065493-6068455 | Colon_Crypt_1 | | SE_24248 | chr19:6065543-6067898 | Colon_Crypt_2 | | SE_25797 | chr19:6054521-6073197 | Duodenum_Smooth_Muscle | | SE_26679 | chr19:6065483-6069956 | Esophagus | | SE_29788 | chr19:6065358-6069204 | Fetal_Muscle | | SE_35921 | chr19:6065744-6068092 | HMEC | | SE_37314 | chr19:6064942-6068309 | HSMMtube | | SE_38048 | chr19:6055954-6068597 | HUVEC | | SE_42288 | chr19:6065246-6069812 | Lung | | SE_44165 | chr19:6064089-6069731 | NHDF-Ad | | SE_44879 | chr19:6065469-6065995 | NHLF | | SE_44879 | chr19:6066023-6067990 | NHLF | | SE_49210 | chr19:6065256-6068547 | Right_Atrium | | SE_52794 | chr19:6065478-6069502 | Small_Intestine | | SE_54507 | chr19:6054642-6073245 | Stomach_Smooth_Muscle | | SE_64265 | chr19:6064909-6067966 | NHEK | | SE_65533 | chr19:6059953-6066138 | Pancreatic_islets | | SE_65533 | chr19:6066252-6068284 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 6066698 | 6067208 | | chr19 | 6067299 | 6067617 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I006055 | chr19 | 6055612 | 6069370 |
|
Enhancer Sequence | GCCGAGGCAG GTGGATCATG AGGTCAGAAG ATCGAGACCA TCCTGGCTAA CACGGTGAAA 60
CCCCGTCTCT ACTACAAATA CAAAAAAATT AGCCGGGTGC GGTGGCGGGC GCCTGTAGTC 120
CCAGCTACTC GGGAGGCTGA GGCGGAAGAA TGGCGTGAAC CCGGGAGGCG GAGCTTCCTG 180
GGCGACAGAA CGAGACTCTG TCTCCAAAAA AAACACAAAT GACATTCCAT TATAAGTTTC 240
TGCTGCAAAA GAAAGTTGGG AAATTTGTTT AGATACTTTA AATAGTCCTA AGATTAGCTG 300
AAATGCCGGT AACAAACGTG CAATGAACAT TTTCTTGGGG GCATTCAGCA ACAAAGTGAA 360
TCGTCCTTAA AAAAAATCCA TACAACTAAA GCGAGTCTCA CCACGGGAAC CACAGGAGCT 420
GTTTTAGTGA GGGGCTGGAG TGTCTGTTAC AGGCGGCACT TTTGCGGCTG TTGCTGCATT 480
AGTCAGATTG CACTCGAGAT GAATGAGGAA GAATAAAGTC TTCACCAAAA ACCTGTCTTG 540
GCTAACAGTT CTGAATTTAT AGCCCTGGCA GTGGGGGCGG GGGCTGGGGG CGGGGCTGGG 600
AGGAGGGGAA GAAATGTGTC ACCCGCTCTG AATGAAGTTC AGGGGTGGTG TTTACCTAAG 660
CAACAAACCC TTGTCAACAA TCGCTATCTC TGGCTTGCCA GCGGAGGAGG TGGGGGAGTG 720
AGGCTGTTTT GATCAAAATC CAACCTGTGG CTGCAAAGTG CCCATCAACA GGGCACTTTG 780
TTAGTGGGAA CGTGCGACCT CTCTTAATAA ACATAACATA CACATCCCAC TGAGGGCCAC 840
GGGTGGACCC AACTTCTTAA CAGGAACATT GAGCACATGA AACCAGAAGG TGCTGGGTCC 900
AATTTCCACC CTCAGCCAAC CCTATCTGTG AATGTCTCTA CATGTGAGCC AGCCAGGGCT 960
CAACTCTTTG CTCTTCTGAA ATTCTTAGGC AGCAGAAATG AAGGCATCGT GCTGAAAAGC 1020
GCTCCAGAAA TTGCGGATTT ATCAGTGATG TACGGTAGTA GGTTGGACAA GTAATGATTT 1080
TCTGAACACC AGGAATTAGA TCAAAAAAGA AATTCCACTT AAGACTAAAA TAAGTCTCCA 1140
GTTGAGAGCA GTCTAGGACA TATTCGAATG GCCAGAAGTT TGTTTCAATG GGGCCTCTGC 1200
GTTTGTGCAG CCTGGGAGTC AACATTACAA TATTGGTTCT TTCAAGCAGA TCCCGAGTGG 1260
ATCCATGTCT GCCTGTTGTG GCAAATCAAA CTCAAATTTA ATCAGAGAAA AATATATGCA 1320
GATGTTCAAT TAAAACCTGG AGTCCGCAGT CTTGGCACTG TTTGCCCGGC CCTCATTGTT 1380
TGCTAAGTAA CAACGGTTGC CAGGGGCAAC GCAGTCCACT CCCGTTTCCA AGAGCCTGTT 1440
GCTGGGCAAC CGGGAGAATA CTTCCCAAAC CAAACAATGT CATCCCGGAG CAACCCCCTC 1500
TATCTCACAT TAACCAGATC TAAAAAAAAC CCTCTCAAAT ATGTAATCTA TTATTTTCAG 1560
AAGCCCTAAG AGAAAGGCAA ATAATCTCTT CTCTATAGTA ACTGAGGGGA AAACAGTTTA 1620
CCATATTTGT TCTGAAATAA CAAAACCCAA GGAGGAACAA CTCTCTCTGA GGTAAGAGGG 1680
CATCACAGGA GGGATTTCAA TCCTTCCTAG TACTGGGAGG AGAAAGTGCC CTTTTCTCCA 1740
AGAGGAAAGA ATCTATTTAT CATCAAACAA ACAATGTGGG AGAGTTCATA GCTGCACAAG 1800
TGTTTTCTGG GCGAAGTAAA ATGAATCATG GATTAAGCTA TTTGGAAAAA AGTGTGAAAA 1860
CAGAGGAGTT GATACCAAAT TAAAACGACT TTTGGAAATA TCATGTACGT ATGGAACAAG 1920
TGCAAAGGGA ACCACTGACT CAGCGTCAGA AATGCCTTGT GGGGCTTTGC CGGGAGGGAC 1980
TTACAGTATA TCTTTGACAT CACTGCGCCG GCTCTTCCCT CCCTACCCGG AGAGAGGAAG 2040
ACTTTTCTAA GAGGAAGCCA GGCCACATCA GATGCCCCCA GATGGCAGGA CACACAAGGG 2100
ACACATATCT CCGGAAAGAG GAGGCACATG GTTGGGCAAT CTCGACCCAT GAAGGGGGAA 2160
AAGAAAAGGG CTAAACTGAA GCTAGTGCAG CTTTTGTTCT GCCTGGAGCA GTTCAGGCTG 2220
AGCATGGCTT CTCTGAGGCT TTGGGACCAG GAGAGGGTGA AGTGGCACCA CCACCTTTCA 2280
AGGGGAACAC AGAGCTCTAA GCAGTGCTCT TGTTTTTGGT GGGCCCAGCC AAGGATCTTA 2340
AAACATTTTG ATAGAATGAG CAACATGTAG CTGCAGCCTC GATGGGTCAA CATTTTGGAT 2400
GATAAAAGCA CACAATGCTG ATAGATTTGT GCATGACCAA GCATACCTTT CAAGGAGCTC 2460
TCAGCGGAGG TTTGCCCTTT GAGACAGACA CAGTCAGTGC ACAGAAACTG TTTTTTTAAG 2520
ATATCATCCA GGAGTCATTC CTAGAATAGG AATGGAATAG ACATGCCTCC CTGAGAAGAA 2580
AGGAAGACAG ATTCTATACT GTTAGAATTT GAATCTGTGT TGCAGGGAGA TGAGGAATTT 2640
GAAGCCAGAC TCTTGGGCTG TTAATGTATG 2670
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