| Tag | Content |
|---|
EnhancerAtlas ID | HS078-01755 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:202014650-202017650 |
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 | CCCAGCTAAT TTTTATGTTT TTACTAGAGA GGGGGTTTCA CCATGTTGGC CAGGATGGTC 60
TCGATCTCCT GAACCTCATG ATCTGCCCAA TTCGGCTTCC CAAAGTGCTG GGATTACAGG 120
TGTGAGCCAC TGCGCCTGGC CAACTGCATG GAGTTTTTAA GATTTCCTAT GGCCCAAGTA 180
CTCATAAGCA TCCTGCATGG ATTAACCCTG AGAGGCAGGT GGTATTATTA TTCTCACTCT 240
ACCTGGGTTC CCACCTGATA ATTGGTGAGG CCCTTTCAAA TGTCCTTTGG CCTTCTATCC 300
CCTGCCTTCT CTTGACTCCT TGAAGTGGGA AAATGAAACC TAAAGTGCCT CCCTCCCCAG 360
AGTGGGCCAT GTGGCGAACT CTATCCAATG TCTCAGCACC TGCCACTCTC TAGTTGCATC 420
CTGGCCATAG GCTGAATGGG TAGGGAGTTC TCTGAGGCTG AGACCATGCT GTGAGGGAGG 480
ATAGGCGGGC CAGGGACAGT GCCAGCAACA GGGACCAGGG AGTGGTGGGA AGGTAAAATA 540
AAGGCAGAGG AAACTTCTCC CAATTGAGGC ACACCTACCC AAGGCCTCTG CCCCTACCCA 600
GACTCCTGAC TTTGACCTGC CTAAAATAAA TCCGGGGTCT GCAAATGGCC TGGAGGCTGC 660
AAATGGCCTG AAGGCTAGTG GTTGGAGGGC AAATAAAGGC AACTCATGGC ACTGCATGCT 720
GCCCCTTGGT GGGCAGGTCC CAGGTCCCAG GGTACCAGCC CCCCTGGGGT GTGATGTGGG 780
CAGCCTCTGA GCTAAGTGAG GTGCAAACAA GAAACCTGGG TTGCCTTTGC CCTCTGTCCG 840
CCCCTTGTCC TCTGTTTACA TCCTCCCTTC CCGTAAATGA GTTGGGTGCT GGGCCCCACT 900
GGCCCTGATC CAGACACACC TGTAGGACAG GTTGGGCAGA GCTCTTGGGG GTGGAGAGCG 960
GGTGGCAGTA CTGGCAGGTG TTTCAGGCCC TTGGGGAGCA AGCTCTGTTC CTTTCCATGG 1020
CAGTGCTGCT GCCAGGCTCT TGCTGCCTTG GGCCAGGAAT TCTTGGCCAA CTCCAAAAGG 1080
ATGGGATGGC TCTAGGGGGG GCTACCTTGC CCAAGGAGTG CCAGGAAGTT GTGTTCAAGC 1140
CCTCAGAGGC AAGAGGACCA AAGGCTCTTT ATCTTCAGTG GGCATTTCCC AGCAGAAATC 1200
TGAGGTCTAG AGCGAGACAG AGTAGAATTG ACAATAAGAT CCACACTTGA GCTGCTAGCT 1260
GCCTTGATGG GAGACCCCAC TGTAACAAGA TGTCCAGGAG GAGGTGGCGG TACTGGGCAC 1320
CCTGGGTGGC TCTGCCTCTC TCTGGACTTT GTTCTGCAGT CAGGTCAGTT GAGGAAGCAA 1380
GAGTGAACCT GGAGTTTGGG TTTCTGGAAG GAGCAAGGGG GAAAGGCAGA CTTGGGCAAG 1440
GGACATAGGT GTCAGATGAG GCAAGTCTGA GTCAGAAGGC AGAGCCTGTG TCCCAGAGGA 1500
AGAGAAACAC CAGTGTCCAG CCTCCAGGCC ACTTGCAGCC CCCAGATTTA TTTTAGGCAG 1560
GTCAAAGTCA GGAGTCTGGG TAGGGGCAGA GGCCTTGGGT GGGTGTGTCT CAACTCAGAG 1620
AAGTTTCCTT TGCCACCAGA GGATTAACTG ACCAAGTTTA CCTAAGATGT GTTTTCCACC 1680
TGATCTCTTC TGTCTCTCTC AACAACAATG ATGACTGTGT ACTCAGTCAA CAAATATGTA 1740
GTAACTGCTT ACTATGTGCC CAGCCCTTTG CTGGGTGCTT AGATCACAGC TGTGTTCATT 1800
GGTGACTTTA CCAATCCATG GCATCATCTC GGTGGGGCAC TGTCCTGGTC AGCTCCTTCT 1860
CCCATTCCCT CCATCACTCC TCCACCCTCA CCTGCAGCTC CTGCATCTCT TGACTCTCAT 1920
CAAATGATCT TGCTGTCTTC TTCACGGGAA GGCCATGACC TCAAACAGGA AATCCTTCAG 1980
TTTCCCACCC TGCTGAATCT GTACCACCTT CCCTCCAGAG GAGTAGAAGA GGTGTCAACC 2040
CTGCCCCCGT GCTGGCGGTC CCAGTCCTGC TCAGCTTCTC TGGACAGGAG ATTAGCACAC 2100
AGAGGCTCAG CTCTAAGACC ACCTAGAGGC CTGCTTTAGG GGGTCCTGCT GAGTAAGGCA 2160
GAGGCTCAGG GTGGCCACAG TGGAGAACTG CTGGCTTAGC CTGCTTCCTG CATTGTGCCT 2220
GAGATGCCTG TGGCAAAGCT TTGCAGTCCC CACACCTGAT TCTGTATGTC CTGGGACACA 2280
ATGACTTGGA TTTCATCTTT TTTTTGTTTT TTCAAGCCAA AAATTAGGAT TCAGTTTATT 2340
CCAACATTGA ATGTATCAGG AAAACCAAAG ATAAAGTGAC AGAGGTACAT TAGGCACACT 2400
GTATACAGAT TTCATCTTTA CTTGACCTTT GCCAAAGAAC TATGCATATT CTGGTGATGG 2460
TGGTTTTCTT CAACAGATCT TTACGGGGAA GGCCCTCTCA TTTCCTCCAC ACCTTTCCTC 2520
TAGTGAAAGC GTTCTCAACC TCCAAGGAGT GTTGGGATTG TCTCCCCAGG TCATATCATC 2580
TGTCATCCAT ATGGGCTGTT AGCTCTGCGA TTTTTGTTCT CAGTCCCCAG GCTGTCTCTC 2640
AGCTCTAGAA GGAATTGTTC AAGGTCCTCC AGGTCCATGG CTCACTGCCT ACTGCCTTTT 2700
CCTTTTAGGG TGGTAAATTA TGGTAAAGTA AATATATGGG GAAACTAACA ATAGATAAGG 2760
ATTATTCAGG ATTTTTTTTG AAACAGGGTT TCACCTGTCA CCCAGGCTGG AGTGCAGTGG 2820
TACAATCTCG GCTCACTGTA ACCTCTACCT CCCAGGTTCA AGAGATTCTT GTGCCTCAGC 2880
CTCCTGAGTA GGTGGGATTA CAGGTTCCCA CCACCACACT GGCTAATTTT TTTTTTTTTT 2940
TTTTTTTGAG ACGGAGTTTC ACTGTTGTTG CCCAGGCTGG AGTGCAATGG TGCGATCTTG 3000
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