| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00354 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:12508770-12511890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR3C1 | MA0113.3 | chr1:12511524-12511541 | AAGGACATTTTGTTCCT | - | 6.08 | | NR3C2 | MA0727.1 | chr1:12511524-12511541 | AAGGACATTTTGTTCCT | - | 6.27 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00009 | chr1:12506389-12526105 | Adipose_Nuclei | | SE_01743 | chr1:12508791-12509347 | Aorta | | SE_01743 | chr1:12509733-12511495 | Aorta | | SE_01743 | chr1:12511532-12515011 | Aorta | | SE_03005 | chr1:12508948-12509464 | Bladder | | SE_03005 | chr1:12509717-12510109 | Bladder | | SE_15065 | chr1:12506299-12515319 | CD4_Memory_Primary_7pool | | SE_20910 | chr1:12506384-12515111 | CD8_Memory_7pool | | SE_26086 | chr1:12506439-12510424 | Duodenum_Smooth_Muscle | | SE_26716 | chr1:12506659-12513255 | Esophagus | | SE_28215 | chr1:12507888-12510030 | Fetal_Intestine | | SE_29231 | chr1:12507637-12510111 | Fetal_Intestine_Large | | SE_29871 | chr1:12507739-12511538 | Fetal_Muscle | | SE_33776 | chr1:12506505-12516452 | HCC1954 | | SE_37319 | chr1:12506164-12510707 | HSMMtube | | SE_39244 | chr1:12508337-12510202 | IMR90 | | SE_39882 | chr1:12506572-12512625 | K562 | | SE_41209 | chr1:12508082-12512128 | Left_Ventricle | | SE_42647 | chr1:12507839-12509412 | Lung | | SE_42647 | chr1:12509663-12511484 | Lung | | SE_42647 | chr1:12511538-12515195 | Lung | | SE_45864 | chr1:12506318-12510756 | Osteoblasts | | SE_49026 | chr1:12508155-12509308 | Right_Atrium | | SE_49026 | chr1:12510064-12511360 | Right_Atrium | | SE_50544 | chr1:12507931-12511360 | Sigmoid_Colon | | SE_51539 | chr1:12506369-12511986 | Skeletal_Muscle | | SE_52815 | chr1:12507938-12510555 | Small_Intestine | | SE_54847 | chr1:12507468-12511742 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012446 | chr1 | 12506572 | 12511845 |
|
Enhancer Sequence | ATTCTACCTG TGTACATCCT GCTTATTTCT GCGGTTTTTA CTTTATAGCA TACTCCACCA 60
ATCCTTTTTA AGGAAAAAGC AAAATCCTAT TATGGGAATG CTTCAAACCA CTCTGAGCTT 120
CCAGATTAAT CTGAAACAGC ATCTGAGTTC ACAACTGGGT CAGAGTTGCA GAATAGCAAG 180
AGAAACTTGC CAGTTCAGCA GGCGTGTGTC TTGGGTTAGT TAAGACAGCA GGACAGTCCT 240
GAGGCCTGAC TTCCTTGCAT GTGTTTCAAC CTTGGGTGCT GAGATAATTC TGGGTGGCTT 300
TAGATAACTT TGTTTCTTAA CTGAAAAAGG AGTGTCTGTT GCCTGATAAG TGTTTATCCG 360
TGAAATAGCA ACATGGTGTG CATCTTAGGG TAGGAGGGCT TTTAGATCTC CAGAGACCAG 420
GAAAAAAAAA AAAGCAAGGT CATTGGCTTA GGCATATTAC TGGAATTAGG ATGTCAGTCC 480
CAACTTTAAA ATGCCTGTAT TGTTTTTATT CAGGGTCCCC TTTCTGGATT CCTCCCCTTT 540
TTTTCTCTTT GCCTTAAGGG CTATACATAA TCCATAACCA AGTAGAACTG AAAACAGACA 600
AAAGCACTCC TCTTCTAGTG GATAGAAATC TGGAATCCAG AAATGCTTCC TTCTTGCCAA 660
ACCTCAACTT GTTCCGTGCC TTTTTTTTTT TTTTAAATGC CTCTTCCCAG CCTCCCCACC 720
CTTTCGTGAT TTGGCTGAGT GAGGACTAGC TGTTTGGTTT GCCTTTTATC AACAATAGAT 780
ATTCACTGCT TTTCAGGTCA CATTTTCCTT TAACTCTTCT CTGTTTATGA GTATCACAAA 840
AGGGTTCTTC AACATCAAGG CAAAACTCAC ACTCAGAATA CTTTTTAACT GTGGATATTT 900
TGACAGTATG AAACGGAAGT CAGTGGTGAA GACTTTCGTT TTGAAGTGAC TTAGGTCTTA 960
CATGACTCAA AGATGGTTTT CCTAGTAGTA TACCAGCAGA GTTGAAAATG ACTCTGAAAT 1020
TGAAAGTCCC ATACTACTTC TAAGAAACTT GTAAAAAGTG TTGGCCAAAT GCTACACCAA 1080
ACATTTTGCA TTAATTATTC TCTTAACTCT TCAAAACAGT CCTTTGCAGG CCAGGCTCGG 1140
TGGCTTATGC CTGTAATCCT AGCACCTCGT GGGGCCGAGG TAGGCAGATC ACATGAAGCC 1200
AGGAGTTCAA GACCAACCTG GCCAACACGG TGAGACCCTG TCTCTACTAA AAATACAAAA 1260
ATTAGCCAGG CGTGGTGGCA CACAACTGTA ATCCCTGCTA CGGGAGGCTG AGGCATGAGA 1320
ACCGCTTGAA CCCAGGAGGT GGAGGTTGCA GTGAGCTGTG ATCGCACCAC TGCACTCCAG 1380
CCTGGGTAAC AGACTGAGAC TCAGCCAGCA AAAAAAAAGA GCAATCCCTT ACAGTAGAAA 1440
GTATGTGATT TTAGCAGATG GATAAACTGA GGTTCAGAGA AATTAAGCCT CTTCCACCAG 1500
CATGCGTGTT TGGTAACTGT CAGGGTAAGA TTTGATTCCT TTGCTCCTGC TTGTTTGACT 1560
ACATCGTGGC AACTCCCACA AAGTTCATGG CAGCCTTACT TAGAGGCACA ATAGATAGTT 1620
GGGTTTTCCA AATTTATGAG TTCAGACATA GCTTATTGCA GGCAATGCTG ATTAGAATTA 1680
GAGCTGTGCT GGTAGCTGAG GTTTGCAGCT GTACAACCTT GTATAGTCTC TGACTTGTGG 1740
TGGTTTAACT TACAATTTTT TGACTTGACG ATGACGTAAA AGCTATATGC ATTCAGTAGA 1800
AACTGTACTT CAGATTTTGA GTTTTGATCT TCCTGGGCTG GTGACATGTG ATCCGATTCT 1860
GTCGCAGTGC TGGGCACTAG GGCAGCCGCA GCTCCTAGTT AGCCACGTGA TCATGAAGAG 1920
GGAACAAATA CTCTACAGTG GGCCCTGCTG CCAGATGACT TCGCCCAGCT GTCAGCTAAT 1980
GTAAGTGTTC CGGGCATGTT TAGATATGTT AGGTGTATGA AATTCATTTT TACTTAAAGC 2040
CTTTTCAACT TAAAAATGGG CTTACCCGGA CGTAATCCCA TCATAAGTCA AGGAGCATCT 2100
GTACTTGGAA GAATATAAAA CTTCTCCATC ACACTACGGA GTCCTGCCAC TTCTCTCTTT 2160
TCCTGTTGTA TTTGGTTACC ATCTTCCCTG GTGACAAGGA AGATACTGCC ACCAGCAATT 2220
ACTCAGTGAG GCAAAGATAT TAAAGAGGAA ATTTCCATTA GGTAAATAAC TGTGAAAGAA 2280
GAACCCAAGA GAAGGGAGAG AAATTCAAGC CCCAGCTCCT GTTACACTGG CCAAATGCCT 2340
TTGGCACCCC ATGCTTGCTG AAGATCATAA AAGGGTCAGG TAAACTGATC AGACAGAACA 2400
GAGGAACACA GTGTGAATTT TTTCCCTTGC CCCATTCCAG TGTCTACTTG AATTTCAGTT 2460
TTAGAAAATC AACCCTTCGG AGCCAGGCCC CAAACCCAGG CTAATTTGCA GTGTCTCCAT 2520
TTGTGTAGAC AATGAGATTA TTTTGGGAAG GAGGGTGTTG ACAGAGTGTG TGTTAGCTAT 2580
TCAGTAGAAC TGGCATCTTG AAGTACTTCT GAGATTTTTA CCCCCTTGCT GAAAATATTG 2640
CTTTATAGAA GTTAATGACT TTGGACTGTG GCCAGAATTC ACAAGTATGG CATGTGTTGA 2700
AGTGAAAGGA AGGGGAAAAT CATTGTCTTT GTGAGTGTAA CACTAGATTT TCTGAAGGAC 2760
ATTTTGTTCC TTGGAACCTT TCATTTTAGC TAGAACAACA TGCACTTGAA GCCTTAAGTA 2820
TTTTGTGGAC TTGAGATTGC TACAAAATGA GGTAGGCAGA CTTAAGTCTC TGCAAATGCT 2880
CCTTCTGGTG TTAAGGTATT ATAACCAAAG AGTTACAAAT TGTCTGCAGA TTACCTTCCA 2940
GTTGCTAGTC GCTTTCCCAG TTTAGAAGCC TAGCACACCC TGGTGCTGTT ATGCCCTGCT 3000
GCAGATAGCT TCCGCTTTGC TGGGGGGATA TGCCATGCCA GATGCTTTAC GTGCACACTA 3060
TCCCTGAATC CTCAAGACAG TCCTGCAGAA TCTGATTATT CCCATTTTGC ATATAAAGAA 3120
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