EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-03975 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr10:134265430-134266850 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR2MA0472.2chr10:134265987-134265998ACGCCCACGCT+6.02
KLF13MA0657.1chr10:134265829-134265847CCTAGAGGGGCGTGACAC-6.4
KLF16MA0741.1chr10:134266447-134266458GGGGGCGGGGC-6.02
KLF5MA0599.1chr10:134266448-134266458GGGGCGGGGC-6.02
NR2C2MA0504.1chr10:134266256-134266271TGACCCCTCACCTCC-6.06
SP1MA0079.4chr10:134266446-134266461GGGGGGCGGGGCCTG-6.65
SP2MA0516.2chr10:134266445-134266462GGGGGGGCGGGGCCTGG-6.26
SP3MA0746.2chr10:134266446-134266459GGGGGGCGGGGCC-6.11
SP4MA0685.1chr10:134266444-134266461GGGGGGGGCGGGGCCTG-6.76
ZNF740MA0753.2chr10:134266442-134266455TTGGGGGGGGCGG-6.54
ZfxMA0146.2chr10:134266447-134266461GGGGGCGGGGCCTG+6.19
ZfxMA0146.2chr10:134265668-134265682GCCGCCTGGGCCTG+6.38
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_09804chr10:134265818-134267072CD14
SE_12419chr10:134265476-134267035CD3
SE_20503chr10:134264308-134267043CD56
SE_23106chr10:134263872-134266728Colon_Crypt_1
SE_23746chr10:134263982-134268555Colon_Crypt_2
SE_24681chr10:134263876-134268448Colon_Crypt_3
SE_27260chr10:134264535-134265597Esophagus
SE_27260chr10:134265747-134266615Esophagus
SE_32166chr10:134263985-134268372Gastric
SE_34405chr10:134265452-134266786HCT-116
SE_41567chr10:134265740-134266705LNCaP
SE_47867chr10:134265830-134266544Pancreas
SE_50630chr10:134264225-134269374Sigmoid_Colon
SE_52741chr10:134264464-134269096Small_Intestine
SE_53287chr10:134265521-134266906Spleen
SE_57559chr10:134265952-134266648VACO_503
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134265015-134267843Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10134266089134266705
Enhancer Sequence
TCCCTGTGGA AGAGCAGGGT GCTGGGTGGG GCATGCTGGG GTGCCGGGAC CCCTGCGCTG 60
GCTGCCACAG TCTGGCAGGG AGCACGCTGC AGCCGCCTGC AGGAGCTGAG CCCAAGGGGA 120
CAGCCGTCCG TGTGTTGGGG AAAGGGGACA GCGATATGTG TGTTGGGGGT GGCCCCGCAT 180
ACCCTCCAGG TAAAGCCATG CACTGTACCT GGGGCGTGGC CCTTGAGTGG CCACTGGAGC 240
CGCCTGGGCC TGAGGGTGGG GTGGGGAGCC CATGTCAGGG TCCAGCCAAA GGTGCCACAG 300
GGCTCCAGCA CCAGAGGCAC CCAGCATGGC CCTGCCTAGC CCTAGGGCCC TCTGCTGCCC 360
AGGGACCCGA CCCTGCAGTC TCTGGGTGGT CAGCGCTGCC CTAGAGGGGC GTGACACCCT 420
CTGCTGGTCC CATACAGAAG GACACAGCTG CCACCCAGCA TGCAGCTCCC CCAGGCACTG 480
GGTGCCCACG CTGTACCCGG CAGCTTACAC TGTGCCTTGT CACCCACGCT GCACCTGGGA 540
GCCCGCACTG TGCCTAGACG CCCACGCTGC GCCTGGGACC TCACACTGCA CGAGGTGCCG 600
GCGCCACTCA GGCAGACCAC CCTCTCCATG TGCGGCAGGA TCCACCAGGG AGGGGCACCC 660
TGACCCTGAT CTCCCCAGGC AGCTCTGGAA AGGCCTGTGT CCTGGCTGGG GACCTCTGGG 720
AGGCCATGGA GCTGGGAGGG AGGGACTGGA GGTCTGAGGG ATCCAAGTAG CCCGTCCTGC 780
TGCACCTGCC AGGCCCCAGT CAGGCCTGGC CATTAAGGCT GAAGGATGAC CCCTCACCTC 840
CTGCCCCTGG GGGCTGAGCC CTACCTAGGA ACCTGAGTGT TTCCAGCACC TCAGCCCTGG 900
CAGTCCCGGC TAGGCAGATC CACCCAGCAC CGTGCAGGAG GCCCCAGGAC TGAGCCCCGC 960
AAGGAACATC TCCCAGTGCC CACAGCCCAC CTAGGGGCCA GTCCACCAGG GATTGGGGGG 1020
GGCGGGGCCT GGGAAGGACA GGGGAAGAGT GAACCACTAG GCCCTGCGTG GCCACTTCCC 1080
AGCAGCCAGA TTTAAGGCCA GGTTAGGATA AATCTCTTGT GCCTCGGTTT CCCCTTCTGT 1140
ACCCCAGGAT CACATTACCC ACCCCCCAAC ACTGTTCTGC AGAATGTGCA GAAAATTGCA 1200
GGTGGTGACG CTTCTGCAAA CAGCAGAGCC CCGGGCACCT GTCCAAGGCG GCTCCGGAAG 1260
GCCCCGCGAG TCCCGTGCGC GGGGACTTCC CAGGGGCGGG GTCGCGGGGC AGGGCGGGCG 1320
CTGGCTCCAC CCCCCGCCGG CCCCGCAGGA ACCGGAAAGG GGCTGGACGG TGTAGCGGCG 1380
CCCCCTGCCG ACACCTCCTA GCATCGCGTC CCCGCGTGGC 1420