| Tag | Content |
|---|
EnhancerAtlas ID | HS032-00093 |
Organism | Homo sapiens |
Tissue/cell | DLD1 |
Coordinate | chr1:202014610-202017540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:202015499-202015511 | CTCTGTTTACAT | - | 6.32 | | FOXP2 | MA0593.1 | chr1:202015500-202015511 | TCTGTTTACAT | - | 6.02 | | IRF2 | MA0051.1 | chr1:202014977-202014995 | GGAAAATGAAACCTAAAG | + | 6.67 | | Znf423 | MA0116.1 | chr1:202015407-202015422 | GCCCCCCTGGGGTGT | - | 6.21 | | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | + | 6.36 | | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | - | 6.66 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:202014631-202017594 | Colon_Crypt_1 | | SE_23723 | chr1:202014745-202017484 | Colon_Crypt_2 | | SE_24689 | chr1:202013412-202017599 | Colon_Crypt_3 | | SE_25977 | chr1:202013680-202018944 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:202014480-202017654 | Esophagus | | SE_27624 | chr1:202013379-202018834 | Fetal_Intestine | | SE_28545 | chr1:202011166-202018857 | Fetal_Intestine_Large | | SE_31432 | chr1:202014570-202017653 | Gastric | | SE_33417 | chr1:202013470-202017710 | H2171 | | SE_33792 | chr1:202014660-202017539 | HCC1954 | | SE_34304 | chr1:202014463-202017386 | HCT-116 | | SE_34741 | chr1:202015302-202017356 | HeLa | | SE_41626 | chr1:202014836-202016985 | LNCaP | | SE_43434 | chr1:202014625-202017551 | MCF-7 | | SE_50066 | chr1:202013466-202017590 | Sigmoid_Colon | | SE_52354 | chr1:202013521-202017654 | Small_Intestine | | SE_56834 | chr1:202014865-202017504 | VACO_400 | | SE_57376 | chr1:202014892-202016968 | VACO_503 | | SE_57945 | chr1:202014917-202016359 | VACO_9m | | SE_57945 | chr1:202016368-202017040 | VACO_9m | | SE_65333 | chr1:202014451-202017286 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 202015600 | 202017009 | | chr1 | 202016172 | 202016526 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I202042 | chr1 | 202011209 | 202018712 |
|
Enhancer Sequence | GCCTCCTGAG TAGCTGGGAT TACAGGCACA CGCAGCCACG CCCAGCTAAT TTTTATGTTT 60
TTACTAGAGA GGGGGTTTCA CCATGTTGGC CAGGATGGTC TCGATCTCCT GAACCTCATG 120
ATCTGCCCAA TTCGGCTTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGCGCCTGGC 180
CAACTGCATG GAGTTTTTAA GATTTCCTAT GGCCCAAGTA CTCATAAGCA TCCTGCATGG 240
ATTAACCCTG AGAGGCAGGT GGTATTATTA TTCTCACTCT ACCTGGGTTC CCACCTGATA 300
ATTGGTGAGG CCCTTTCAAA TGTCCTTTGG CCTTCTATCC CCTGCCTTCT CTTGACTCCT 360
TGAAGTGGGA AAATGAAACC TAAAGTGCCT CCCTCCCCAG AGTGGGCCAT GTGGCGAACT 420
CTATCCAATG TCTCAGCACC TGCCACTCTC TAGTTGCATC CTGGCCATAG GCTGAATGGG 480
TAGGGAGTTC TCTGAGGCTG AGACCATGCT GTGAGGGAGG ATAGGCGGGC CAGGGACAGT 540
GCCAGCAACA GGGACCAGGG AGTGGTGGGA AGGTAAAATA AAGGCAGAGG AAACTTCTCC 600
CAATTGAGGC ACACCTACCC AAGGCCTCTG CCCCTACCCA GACTCCTGAC TTTGACCTGC 660
CTAAAATAAA TCCGGGGTCT GCAAATGGCC TGGAGGCTGC AAATGGCCTG AAGGCTAGTG 720
GTTGGAGGGC AAATAAAGGC AACTCATGGC ACTGCATGCT GCCCCTTGGT GGGCAGGTCC 780
CAGGTCCCAG GGTACCAGCC CCCCTGGGGT GTGATGTGGG CAGCCTCTGA GCTAAGTGAG 840
GTGCAAACAA GAAACCTGGG TTGCCTTTGC CCTCTGTCCG CCCCTTGTCC TCTGTTTACA 900
TCCTCCCTTC CCGTAAATGA GTTGGGTGCT GGGCCCCACT GGCCCTGATC CAGACACACC 960
TGTAGGACAG GTTGGGCAGA GCTCTTGGGG GTGGAGAGCG GGTGGCAGTA CTGGCAGGTG 1020
TTTCAGGCCC TTGGGGAGCA AGCTCTGTTC CTTTCCATGG CAGTGCTGCT GCCAGGCTCT 1080
TGCTGCCTTG GGCCAGGAAT TCTTGGCCAA CTCCAAAAGG ATGGGATGGC TCTAGGGGGG 1140
GCTACCTTGC CCAAGGAGTG CCAGGAAGTT GTGTTCAAGC CCTCAGAGGC AAGAGGACCA 1200
AAGGCTCTTT ATCTTCAGTG GGCATTTCCC AGCAGAAATC TGAGGTCTAG AGCGAGACAG 1260
AGTAGAATTG ACAATAAGAT CCACACTTGA GCTGCTAGCT GCCTTGATGG GAGACCCCAC 1320
TGTAACAAGA TGTCCAGGAG GAGGTGGCGG TACTGGGCAC CCTGGGTGGC TCTGCCTCTC 1380
TCTGGACTTT GTTCTGCAGT CAGGTCAGTT GAGGAAGCAA GAGTGAACCT GGAGTTTGGG 1440
TTTCTGGAAG GAGCAAGGGG GAAAGGCAGA CTTGGGCAAG GGACATAGGT GTCAGATGAG 1500
GCAAGTCTGA GTCAGAAGGC AGAGCCTGTG TCCCAGAGGA AGAGAAACAC CAGTGTCCAG 1560
CCTCCAGGCC ACTTGCAGCC CCCAGATTTA TTTTAGGCAG GTCAAAGTCA GGAGTCTGGG 1620
TAGGGGCAGA GGCCTTGGGT GGGTGTGTCT CAACTCAGAG AAGTTTCCTT TGCCACCAGA 1680
GGATTAACTG ACCAAGTTTA CCTAAGATGT GTTTTCCACC TGATCTCTTC TGTCTCTCTC 1740
AACAACAATG ATGACTGTGT ACTCAGTCAA CAAATATGTA GTAACTGCTT ACTATGTGCC 1800
CAGCCCTTTG CTGGGTGCTT AGATCACAGC TGTGTTCATT GGTGACTTTA CCAATCCATG 1860
GCATCATCTC GGTGGGGCAC TGTCCTGGTC AGCTCCTTCT CCCATTCCCT CCATCACTCC 1920
TCCACCCTCA CCTGCAGCTC CTGCATCTCT TGACTCTCAT CAAATGATCT TGCTGTCTTC 1980
TTCACGGGAA GGCCATGACC TCAAACAGGA AATCCTTCAG TTTCCCACCC TGCTGAATCT 2040
GTACCACCTT CCCTCCAGAG GAGTAGAAGA GGTGTCAACC CTGCCCCCGT GCTGGCGGTC 2100
CCAGTCCTGC TCAGCTTCTC TGGACAGGAG ATTAGCACAC AGAGGCTCAG CTCTAAGACC 2160
ACCTAGAGGC CTGCTTTAGG GGGTCCTGCT GAGTAAGGCA GAGGCTCAGG GTGGCCACAG 2220
TGGAGAACTG CTGGCTTAGC CTGCTTCCTG CATTGTGCCT GAGATGCCTG TGGCAAAGCT 2280
TTGCAGTCCC CACACCTGAT TCTGTATGTC CTGGGACACA ATGACTTGGA TTTCATCTTT 2340
TTTTTGTTTT TTCAAGCCAA AAATTAGGAT TCAGTTTATT CCAACATTGA ATGTATCAGG 2400
AAAACCAAAG ATAAAGTGAC AGAGGTACAT TAGGCACACT GTATACAGAT TTCATCTTTA 2460
CTTGACCTTT GCCAAAGAAC TATGCATATT CTGGTGATGG TGGTTTTCTT CAACAGATCT 2520
TTACGGGGAA GGCCCTCTCA TTTCCTCCAC ACCTTTCCTC TAGTGAAAGC GTTCTCAACC 2580
TCCAAGGAGT GTTGGGATTG TCTCCCCAGG TCATATCATC TGTCATCCAT ATGGGCTGTT 2640
AGCTCTGCGA TTTTTGTTCT CAGTCCCCAG GCTGTCTCTC AGCTCTAGAA GGAATTGTTC 2700
AAGGTCCTCC AGGTCCATGG CTCACTGCCT ACTGCCTTTT CCTTTTAGGG TGGTAAATTA 2760
TGGTAAAGTA AATATATGGG GAAACTAACA ATAGATAAGG ATTATTCAGG ATTTTTTTTG 2820
AAACAGGGTT TCACCTGTCA CCCAGGCTGG AGTGCAGTGG TACAATCTCG GCTCACTGTA 2880
ACCTCTACCT CCCAGGTTCA AGAGATTCTT GTGCCTCAGC CTCCTGAGTA 2930
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