| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02950 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:202014710-202017570 |
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 | TCGATCTCCT GAACCTCATG ATCTGCCCAA TTCGGCTTCC CAAAGTGCTG GGATTACAGG 60
TGTGAGCCAC TGCGCCTGGC CAACTGCATG GAGTTTTTAA GATTTCCTAT GGCCCAAGTA 120
CTCATAAGCA TCCTGCATGG ATTAACCCTG AGAGGCAGGT GGTATTATTA TTCTCACTCT 180
ACCTGGGTTC CCACCTGATA ATTGGTGAGG CCCTTTCAAA TGTCCTTTGG CCTTCTATCC 240
CCTGCCTTCT CTTGACTCCT TGAAGTGGGA AAATGAAACC TAAAGTGCCT CCCTCCCCAG 300
AGTGGGCCAT GTGGCGAACT CTATCCAATG TCTCAGCACC TGCCACTCTC TAGTTGCATC 360
CTGGCCATAG GCTGAATGGG TAGGGAGTTC TCTGAGGCTG AGACCATGCT GTGAGGGAGG 420
ATAGGCGGGC CAGGGACAGT GCCAGCAACA GGGACCAGGG AGTGGTGGGA AGGTAAAATA 480
AAGGCAGAGG AAACTTCTCC CAATTGAGGC ACACCTACCC AAGGCCTCTG CCCCTACCCA 540
GACTCCTGAC TTTGACCTGC CTAAAATAAA TCCGGGGTCT GCAAATGGCC TGGAGGCTGC 600
AAATGGCCTG AAGGCTAGTG GTTGGAGGGC AAATAAAGGC AACTCATGGC ACTGCATGCT 660
GCCCCTTGGT GGGCAGGTCC CAGGTCCCAG GGTACCAGCC CCCCTGGGGT GTGATGTGGG 720
CAGCCTCTGA GCTAAGTGAG GTGCAAACAA GAAACCTGGG TTGCCTTTGC CCTCTGTCCG 780
CCCCTTGTCC TCTGTTTACA TCCTCCCTTC CCGTAAATGA GTTGGGTGCT GGGCCCCACT 840
GGCCCTGATC CAGACACACC TGTAGGACAG GTTGGGCAGA GCTCTTGGGG GTGGAGAGCG 900
GGTGGCAGTA CTGGCAGGTG TTTCAGGCCC TTGGGGAGCA AGCTCTGTTC CTTTCCATGG 960
CAGTGCTGCT GCCAGGCTCT TGCTGCCTTG GGCCAGGAAT TCTTGGCCAA CTCCAAAAGG 1020
ATGGGATGGC TCTAGGGGGG GCTACCTTGC CCAAGGAGTG CCAGGAAGTT GTGTTCAAGC 1080
CCTCAGAGGC AAGAGGACCA AAGGCTCTTT ATCTTCAGTG GGCATTTCCC AGCAGAAATC 1140
TGAGGTCTAG AGCGAGACAG AGTAGAATTG ACAATAAGAT CCACACTTGA GCTGCTAGCT 1200
GCCTTGATGG GAGACCCCAC TGTAACAAGA TGTCCAGGAG GAGGTGGCGG TACTGGGCAC 1260
CCTGGGTGGC TCTGCCTCTC TCTGGACTTT GTTCTGCAGT CAGGTCAGTT GAGGAAGCAA 1320
GAGTGAACCT GGAGTTTGGG TTTCTGGAAG GAGCAAGGGG GAAAGGCAGA CTTGGGCAAG 1380
GGACATAGGT GTCAGATGAG GCAAGTCTGA GTCAGAAGGC AGAGCCTGTG TCCCAGAGGA 1440
AGAGAAACAC CAGTGTCCAG CCTCCAGGCC ACTTGCAGCC CCCAGATTTA TTTTAGGCAG 1500
GTCAAAGTCA GGAGTCTGGG TAGGGGCAGA GGCCTTGGGT GGGTGTGTCT CAACTCAGAG 1560
AAGTTTCCTT TGCCACCAGA GGATTAACTG ACCAAGTTTA CCTAAGATGT GTTTTCCACC 1620
TGATCTCTTC TGTCTCTCTC AACAACAATG ATGACTGTGT ACTCAGTCAA CAAATATGTA 1680
GTAACTGCTT ACTATGTGCC CAGCCCTTTG CTGGGTGCTT AGATCACAGC TGTGTTCATT 1740
GGTGACTTTA CCAATCCATG GCATCATCTC GGTGGGGCAC TGTCCTGGTC AGCTCCTTCT 1800
CCCATTCCCT CCATCACTCC TCCACCCTCA CCTGCAGCTC CTGCATCTCT TGACTCTCAT 1860
CAAATGATCT TGCTGTCTTC TTCACGGGAA GGCCATGACC TCAAACAGGA AATCCTTCAG 1920
TTTCCCACCC TGCTGAATCT GTACCACCTT CCCTCCAGAG GAGTAGAAGA GGTGTCAACC 1980
CTGCCCCCGT GCTGGCGGTC CCAGTCCTGC TCAGCTTCTC TGGACAGGAG ATTAGCACAC 2040
AGAGGCTCAG CTCTAAGACC ACCTAGAGGC CTGCTTTAGG GGGTCCTGCT GAGTAAGGCA 2100
GAGGCTCAGG GTGGCCACAG TGGAGAACTG CTGGCTTAGC CTGCTTCCTG CATTGTGCCT 2160
GAGATGCCTG TGGCAAAGCT TTGCAGTCCC CACACCTGAT TCTGTATGTC CTGGGACACA 2220
ATGACTTGGA TTTCATCTTT TTTTTGTTTT TTCAAGCCAA AAATTAGGAT TCAGTTTATT 2280
CCAACATTGA ATGTATCAGG AAAACCAAAG ATAAAGTGAC AGAGGTACAT TAGGCACACT 2340
GTATACAGAT TTCATCTTTA CTTGACCTTT GCCAAAGAAC TATGCATATT CTGGTGATGG 2400
TGGTTTTCTT CAACAGATCT TTACGGGGAA GGCCCTCTCA TTTCCTCCAC ACCTTTCCTC 2460
TAGTGAAAGC GTTCTCAACC TCCAAGGAGT GTTGGGATTG TCTCCCCAGG TCATATCATC 2520
TGTCATCCAT ATGGGCTGTT AGCTCTGCGA TTTTTGTTCT CAGTCCCCAG GCTGTCTCTC 2580
AGCTCTAGAA GGAATTGTTC AAGGTCCTCC AGGTCCATGG CTCACTGCCT ACTGCCTTTT 2640
CCTTTTAGGG TGGTAAATTA TGGTAAAGTA AATATATGGG GAAACTAACA ATAGATAAGG 2700
ATTATTCAGG ATTTTTTTTG AAACAGGGTT TCACCTGTCA CCCAGGCTGG AGTGCAGTGG 2760
TACAATCTCG GCTCACTGTA ACCTCTACCT CCCAGGTTCA AGAGATTCTT GTGCCTCAGC 2820
CTCCTGAGTA GGTGGGATTA CAGGTTCCCA CCACCACACT 2860
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