EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS140-00973 
Organism
Homo sapiens 
Tissue/cell
Namalwa 
Coordinate
chr14:106046870-106050010 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr14:106047139-106047150TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047243-106047254TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047284-106047295TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047367-106047378TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047408-106047419TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047487-106047498TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047530-106047541TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047573-106047584TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047659-106047670TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047702-106047713TCTTATCTCTC+6.32
Gata4MA0482.1chr14:106047743-106047754TCTTATCTCTC+6.32
Nfe2l2MA0150.2chr14:106048505-106048520CACAATGACTCAGCC+6.23
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_10157chr14:106046012-106056780CD19_Primary
SE_10848chr14:106045899-106056875CD20
SE_20287chr14:106046034-106050248CD56
SE_32465chr14:106046001-106049884GM12878
SE_33471chr14:106046042-106049462H2171
SE_33471chr14:106049513-106051403H2171
SE_43513chr14:106046025-106053457MM1S
SE_50289chr14:106046123-106051407Sigmoid_Colon
SE_53003chr14:106046524-106047301Small_Intestine
SE_53003chr14:106047520-106050526Small_Intestine
SE_54039chr14:106046471-106047271Spleen
SE_54039chr14:106047661-106050001Spleen
SE_58507chr14:106025162-106072855Ly1
SE_58987chr14:106025160-106052426Ly3
SE_60483chr14:106024968-106056362DHL6
SE_61472chr14:106025167-106070246Toledo
SE_67193chr14:106046025-106053457MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14106047540106049530
Number: 2             
IDChromosomeStartEnd
GH14I105580chr14106046900106049495
GH14I105583chr14106049514106051403
Enhancer Sequence
AATGTTGTAT AATAGTCGTG GTGTGTGTTT GTGAGTATGA CTGTGTGAGA GGGGCTTGCA 60
CCTGAGTTCC TGGGCCCATC TTGCTGCCTC TTTCTCTCCC TGTGTGTTCT CTGCCTCTGT 120
TGTGTTCTCT CTGCATGTCT GTCTCCATGT CTCTTTTTCC CTGTTCCCAT CTCCTCCCTT 180
TTTCTCCCAT CTCTGTCTCT GTTTCTTATC TATCTCATCT CATCTCTCTC TTTCTGTCTC 240
TTGTGTCTCT GTCCCTCCCC GTCCCTGTCT CTTATCTCTC TCCATCCCCA TCTCTCTCTC 300
TGTGTCTGTC TTTGTCCCTG TCTCTATGTC TCTTGTCTCT CCCCATCCCT GTCTCTCTCT 360
ATGTCTCTGT GTCTCTTATC TCTCCCCATC CCTGTCTCTC TATGTCTCTG TGTCTCTTAT 420
CTCTCCTTGT CCTTGTCTTT CTCTGTCTAC GTCTCTGTGT CTCTCTCCAT CCCTGTCTCT 480
CTCTATGTCT CTGTGTCTCT TATCTCTCCC CATCCCTGTC TCTCTATGTC TCTGTGTCTC 540
TTATCTCTCC TTGTCCTTGT CTTTCTCTGT CTATGTCTCT GTGTCTCTCC CCATCCCTGT 600
CTCTCTCTCT CTGTGTCTCT TATCTCTCCC CATCCCTGTC TCTCTCTATG TCTCTTCATC 660
TCTTATCTCT CTCCCCATCC CTGTCTCTCT ATGTCTCTAT GTCTCTTATC TCTCCTTGTC 720
CTTGTCTTTC TCTGTCTATG TCTCTTGTCT CTCCCCATCC CTGTCTCTCT CTCTCTATGT 780
CTCTGTGTCT CTTATCTCTC CCCATCCCTG TCTCTCTCTA TGTCTCTTCA TCTCTTATCT 840
CTCTCCCCAT CCCTGTCTCT ATGTCTCTGT GTCTCTTATC TCTCCCCATC CTTGTCTCTG 900
TCTATGTCTC TGTGTCTCTT GTCTCTCCCT GTCCCTGTCT CTCTCTATGT CTCTGTGTCT 960
CTCTGGGCCC CTGGTCCAAT GTCCCCTTCC CAGAACCCCT GTTTCCCTGG TGTGGGGTGC 1020
AGGTCCTTCT GTGGTCCTGT GGGCCGTGCT TGTGCTGGGC ACAGCCTGCC AGGGCAGCCG 1080
CTCAAGCCCC AGGGCTGGGC ACTGCGTCCT GGCTCTGGCC AAGGGCCCTG GGGAGAGCTG 1140
AGGGAGGTGC GTGCAGGGTG TGAGGCCCAC CACAGTCACT GCCAGATGCT CAGTGCTGGT 1200
GCTTCCCTGG GTCTGCTGTG TGGTGGGCAC AGCCCTCGTG AGGGCTGCCC ATGGAGGAGG 1260
CCTGCCGCCT AGAGAGCCCG GACAGGGGGA CAATGGCCTG TGCTGACCCT GGCGGAACCC 1320
TGGCTGACCC CAGATGACCC CAGATGGCCC TGGCTGACCC TGGCGGAACC CAGATGACCC 1380
TGGCTGACCC TGGCTGGCCC TGGCTGACCC CAGATGACCC TGGCTGACCC TGGCTGATCC 1440
TGGCTGACCC TGGCTGACCT CTGCCTAACC CTGGACCTGG AAAGCCCTAG CTGACCCCGG 1500
GCTGGTTGGG GCTGGGCCTC CCTGTGGCTG CAGCCCCTCG CTCAGGCCCC AGGCACACCT 1560
GGCCAGGTCT CGGTTTTGGG GCATGTTTCT CAGAACAGCA GTTCTCTGGC TGGAACACCT 1620
GGCCTGGGCT GTGTTCACAA TGACTCAGCC GCCCCACAGG GCTATTTTGG ATATTTCTGC 1680
AGGTGATGGG GTACAAGAGG CTTCAGGAGA GAGAGAAAAG CAAGAGAATA CAAACAGCAT 1740
GGCCTCCCCC GACCTTCCTG TCCCCACTCC TGTACTGTAC CCCCTCCCCA GTGCTAAGTC 1800
GAGACCTGGC GACCCCTTAG GGGCTGGGGC TGGGTGTAGC TCACAGGGCC TGGGCTGGTC 1860
CTCTCCCCAC CAAGTCCTCC TGGGGCCTAC ACACCCCTCT GAGCCTGGAA AAATGGAGCA 1920
AGTCATTGGG GTCATTTCTT CATCTACCAG TGAGTACATG CACTGAGAGG GTCTCGGCTC 1980
CCCTGGAGGC CTCCCTCCAC CACTGCAGGT CACTTACTCA TGAGGGCCAA GGCTCAGAAA 2040
TCAGACAGGA CTCAGTGTCT AGTCAGACTG ATACATGCTC AGAAAAGGAA TCAGATTTCA 2100
AAATGAATAT GTATAAGAAA AGAACCGGGG ATCAGTGATC AGGAACAGGG ATCCATGATC 2160
TGGTCCAGGG CTCAGCGGTC AGGAACAGGG CCCAGCGATC AGGACCAGGG CTCAGTAATC 2220
AGGACCAGGG CCCAGTGATC AGGACCAGGG CCCAGCGATT GGGTCCAGGG CTCAGTGATC 2280
AGGAACAGGG CTCAGTGATC AGGACCAGGG CCCAGTGATC AGGAACAGGG GCCAGTGACT 2340
GGGTCCAGGG CTCAGTAATC AGGACCAGGG CTCAGTGATC AGGACCAGGG CTCAGTGATC 2400
AGGAACAGGG GTTAGTGATC AGGAACAGGG CTCAGTGATC AGGACCAGCA TTCAGTGATC 2460
AGGACCAGGG CTCAGTGATC AGGAACAGGG CTGAGTGACC AGGACCAGGG CTGAGTGATC 2520
AGGTCCAGGG CTGAGTGATG AGGACCAGGG CTGAGTGAGG AGGTCCAGGG CTGAGTGATG 2580
AGGTCCAGGG CTGAGTGACG AGGTCCAGGG CTGAGTGACG AGGACCAGGG CTGAGTGACG 2640
AGGTCCAGGG CTGAGTGACG AGGACCAGGG CTGAGTGACC AGGACCAGGG CTGAGTGATG 2700
AGGTCCAGGG CTGAGTGACA AGGACCAGGG CTGAGTGACG AGGTCCAGGG CAAAAAACAG 2760
GAGTAGGACT CAGTGATCAG GACTAAGGCT CAGTGATCAA GGCTAGAATT AAGTGATCAG 2820
GAACAGGGAC CAAGTAGTAG GACCAGAGCT CAGTGATCGG TAAACGGGCC CACTGGTCAG 2880
GACCAGGGCC CTGTGATCAG GATGAGGACC CAGTGAGGAG GACCAGGGCT GTCTAGGTTA 2940
TGAGGAATAG GGATCCCATG TAGTTCTTAG GAGCAGGCTT CTTTGCCATG GTCTCTGGTG 3000
AATCCAGCAT TCATCCTTGG GCCTCAGCCT CATTCAAGAT CAGGTCATTT CTTGATTTTG 3060
GGACCAGGGG TACCCTCTGT CCATGCCCAC CATGACCACC ATGACACCCA GGGGGACTTT 3120
GAAGCAGGCG TTCTCCAGTC 3140