| Tag | Content |
|---|
EnhancerAtlas ID | HS116-32250 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr7:137669430-137672100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr7:137671725-137671736 | CTGCAGCTGTT | - | 6.02 | | TCF3 | MA0522.2 | chr7:137670465-137670475 | AACACCTGCT | + | 6.02 | | Tcf12 | MA0521.1 | chr7:137671725-137671736 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00066 | chr7:137667589-137682153 | Adipose_Nuclei | | SE_01161 | chr7:137670669-137672074 | Adrenal_Gland | | SE_01583 | chr7:137664394-137670602 | Aorta | | SE_01583 | chr7:137670747-137675600 | Aorta | | SE_06592 | chr7:137657869-137670517 | Brain_Hippocampus_Middle | | SE_06592 | chr7:137670557-137675748 | Brain_Hippocampus_Middle | | SE_25824 | chr7:137667762-137673330 | Duodenum_Smooth_Muscle | | SE_27287 | chr7:137670706-137672046 | Esophagus | | SE_27744 | chr7:137667496-137672283 | Fetal_Intestine | | SE_28585 | chr7:137667434-137674722 | Fetal_Intestine_Large | | SE_30032 | chr7:137671119-137672415 | Fetal_Muscle | | SE_32391 | chr7:137669962-137670512 | Gastric | | SE_32391 | chr7:137670737-137673270 | Gastric | | SE_35591 | chr7:137667788-137673582 | HepG2 | | SE_37226 | chr7:137670234-137672408 | HSMMtube | | SE_39130 | chr7:137670746-137672605 | IMR90 | | SE_44792 | chr7:137669773-137670254 | NHLF | | SE_44792 | chr7:137670565-137673332 | NHLF | | SE_45544 | chr7:137657492-137687859 | Osteoblasts | | SE_46995 | chr7:137670989-137671893 | Ovary | | SE_50455 | chr7:137667391-137675519 | Sigmoid_Colon | | SE_51841 | chr7:137670769-137672194 | Skeletal_Muscle_Myoblast | | SE_52498 | chr7:137664427-137676040 | Small_Intestine | | SE_55864 | chr7:137671360-137672913 | u87 | | SE_59162 | chr7:137664421-137694313 | Ly3 | | SE_61141 | chr7:137663463-137694162 | HBL1 | | SE_61912 | chr7:137664409-137678967 | Toledo | | SE_63629 | chr7:137670708-137673152 | HSMM |
|
| | 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 |
| GH07I137974 | chr7 | 137659055 | 137680050 |
|
Enhancer Sequence | TTTGTTTGGT TTTTCTAAAA GCAAACTTGG GTCGAGTAAT AGTTCCTCAA AAAAGCTATG 60
GGGGAATAAA AAATCTACCT ACCAGGATAT TTTTCTTTCG GTTGGCAAAT ACCAAAGAAC 120
AAACTTCTCC ATGAAAGGAG TCTGCGTTTC ATGAAAGATC AAAGGTCTCA AAGTCTCCCA 180
AATTGCAAAC TCTTCTACAG TAACGTAGCC CAGTAGAGAA GAGCCATCAG GCAGCTCATT 240
AAAGCTTGTC AGCCTCAATA GCTAACATTT TCTTCCTTTC TCATTGAACT CCATTATCAG 300
CAATGAGTTT TGCGGGGAGC TGGGGGTTTT GTTTGTTTTC TTTTGCTTTT ACTTAAAATA 360
AAAATGTGTA ACTTAACTTC CAAGAGACAT TGAGATTTGG GCACAGTTTT CAGTCAGCTC 420
CCTCTTCAAA GACCTACTGC AATTGCCAAA GCAATAATAA GACATTATGG AAAGGGGGAA 480
GGGGGCCCAT TCACACGCCA GAATCTCCAT ATAACCTCTG TTTGATAAAA TGCTAGTTGG 540
TCCAGATAAA TGGAAGGCAC AGGAGAGCAA CTTAGAACCT GATTCCCAAG AAAGCAGGAC 600
TCAGAGAGGT TCTCTCGCTC AACAATATGT ACATCAACTG CTTGGGAACA GCCAAGGCTA 660
GACGCAGTTC AGGCCAGGGG TCGGAGGAAG AACGTGGCTT AAATGCCTTT GCTGCAGTGT 720
ATGGACAGCA TTCCAAAGGT GCTCTGCCAG GAAGCCCCAG GCCTCGTGGA TGGAGAGCGC 780
TTCAGCTTGT CCCTGACACT GCAGGCAGTA GCCCTACCAG GACTGCTCAG TGCCATCCTG 840
CTGTCCCCTA CTCACCTTCC TGCTGTTAAC AGACCCCTAA ACAGGTCACA ATCAGCCCCA 900
GAAAGACTAT TTTCATTAGG AAAAAATAAT GTAAGTGACC TCAGTGTCCA GTGATAGATG 960
GTGTTTCAGG AAATGACAGG GACATGGAAC AAGCCGTCCC CTTCTTGTCT TCCCTCTTGT 1020
AACTTAAAGA GTGCTAACAC CTGCTGCCAA CCCACCCCCT CAAAACTGAC AAAAACATTT 1080
CAGTTCCTCA GAAGCAGGTG CCTGAAAATT TGAAGTGTTA ATTCAGTCAT GCAAATCAAT 1140
ACCAGGCGTT GAACCTAAGA GGATTCAGGT AAGAACTGAA GAAATATTTC AGGTCTTTTT 1200
CCCTAAATGC CTTTCACAAT TAGGCCACAA TTCAGAGGTC TTATTCTATT TACTCATTTT 1260
ATCCATGAGT TCAGAATGCA GCAAAAATTT TCTTCCTAGG CCTCTCAGAA ACTATTGGAG 1320
AAAAAAAAAT AGAAGAAAGG AACCGAATAT CCCCCATCTA GCGGCCACAA ACCAGACATA 1380
GTGACACTTT ACTTATGTCA TTTATCTTCC TCCACCATGG CCTTGTGAAA CAGTCTCAGA 1440
AAGGTGCTCA CAGTAGGGAG AGCCAGAACC AGATTGTAAG CCTAGACTCA TTCATTTGTT 1500
CATCCATTCA TTCACCAAAC ATTTTACTGG ACACCTACCA TGCGCACAGC ACTGTTCTGT 1560
TAGCTGGAGA TAAACAGCAG TGAATAAAAG AAAGTCTCTG CTTTCACGGT GTTTCCATTT 1620
TGTTAGACGA GAAAACAGAC AAGCACACTT ATCAGGGCTT CCCAACAGGT ATGCCGGGGA 1680
GTGCCCCAGC TCCATGGGAC TGGGAAGGAG GGCAAGTTGG CAGCAGAGGC TGGAGCGACT 1740
GCACCCCTGA GATGGATTCC ACCCACTATG ATTAGGCTCA TCCATTACTT TGACACAAAG 1800
CACCATGCAG ATATCATCAT TTTCCATGAC TGCCATGACA GCAGGGCTCG GGGATACTAA 1860
AGAAATCATT TGCCAGTGGT GATAAGGGCT ATGAAGTTGT GCTGACCGCA AAATCCCTGC 1920
TCCTCCTACC AACTGCCTTT TCCAGTGGTT GAGCAATCTG CAGACAAGAG GACAGTCAGA 1980
ATCCCACACC GAAACTGGGA GGGTGGGAAT AAGAAGCTGA AACTTCCTCA TGCTCCATCT 2040
ACCCAGCCAT CCCACCCTCA TTTCAGTGTC CTCCTAGAAG TCTGTATTTC AGTCAAAAGG 2100
AAACACTGGA TTTCGACGTG CCTCATGTTC CTCAGCTTGT AAACACAGCT GAGAAACCAA 2160
ATGGTTTTTT GGCAGCTACG TTTCTGCCCC TCTCTTAGCA CACAAGAAAA CGTGTCTGTG 2220
AAGACTGCCT TAGAACATGA TGCCTCGAGC CCAAGGGCGA CCCCACTGCA CCATGCAGGT 2280
AACATCACAG CTGTGCTGCA GCTGTTCGCC TGGAGCTGGT TTGGGCCTTG GCCTCCTCAG 2340
CCCACTGCCC CAGCTCTCCC AGCGGCTCCA ACATGGGTCT TGGGCTGCAG GAGAGCCTGG 2400
AGAGAAAGCT TGCAAACCCA GAGTGGAACC AGAAAAACAA TTCCTGGCAG TGCCTCAGAA 2460
ATGAATACCA TTCAGGGGTA GGAAGTAAAA AGTCAAAACT ACAAAGATCG GAGTCAGGTT 2520
CTTTGGTTAC AAAAAATATA TACTGTTTCC TCACTAGATC CCATCTCTTT CCAAAGGATA 2580
ACATCTACTG CCTAAGTCAT CTGTAACTGG AAAGAGGGAG GGAAATGCCG CACCACAGTT 2640
TGACTTTTTA ATGGTACTGA AATCTATAGG 2670
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