EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-20080 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr5:131810000-131811350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11741255chr5131811182hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr5:131810769-131810790GATGGAGGAGGGGGAAGGTAA+6.27
ZNF263MA0528.1chr5:131810303-131810324CCTTCTGCCTCCTCCTTCTTC-6.44
ZNF263MA0528.1chr5:131810772-131810793GGAGGAGGGGGAAGGTAAGGC+6.63
ZNF263MA0528.1chr5:131810766-131810787GGAGATGGAGGAGGGGGAAGG+6.65
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00037chr5:131810090-131812540Adipose_Nuclei
SE_01257chr5:131810577-131811720Adrenal_Gland
SE_04124chr5:131810599-131811590Brain_Anterior_Caudate
SE_06435chr5:131810039-131812439Brain_Hippocampus_Middle
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131806085-131811485CD3
SE_14495chr5:131805826-131811661CD4_Memory_Primary_7pool
SE_16304chr5:131807811-131811139CD4_Naive_Primary_8pool
SE_17370chr5:131804876-131811594CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131804786-131818044CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131805804-131811428CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131810146-131811550CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131810171-131811664CD8_Memory_7pool
SE_21960chr5:131806740-131810211CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23079chr5:131810420-131815180Colon_Crypt_1
SE_23750chr5:131810479-131811551Colon_Crypt_2
SE_25340chr5:131808656-131817904DND41
SE_25784chr5:131810212-131813275Duodenum_Smooth_Muscle
SE_26597chr5:131810388-131811474Esophagus
SE_27629chr5:131808629-131817861Fetal_Intestine
SE_28559chr5:131808476-131817875Fetal_Intestine_Large
SE_30917chr5:131809910-131811467Fetal_Thymus
SE_31393chr5:131810363-131811622Gastric
SE_39368chr5:131809998-131811728Jurkat
SE_40726chr5:131809980-131815612Left_Ventricle
SE_42103chr5:131809951-131815230Lung
SE_48659chr5:131810417-131814893Right_Atrium
SE_50023chr5:131810017-131811707RPMI-8402
SE_50051chr5:131808593-131816260Sigmoid_Colon
SE_52336chr5:131808690-131816220Small_Intestine
SE_53285chr5:131809900-131816337Spleen
SE_54554chr5:131810068-131812535Stomach_Smooth_Muscle
SE_55171chr5:131810920-131811233Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131810440-131811582Pancreatic_islets
SE_66244chr5:131809998-131811728Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131810095131810374
chr5131810202131811200
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GCAATCTGCC TGCCTCAGCC TCCCAAAGTG CTAGGATTAC AGGTGTAAGC CACTGCACCT 60
GGCCCGTTTC TTTTCTTATA GTTCTGTAGT CAGAAGTCCA AAACAGGTCT CACTGGGCTA 120
AACTCAAGGT GTCAACAGAG CTGCATTTCT TCCTGGGGGC TCTAGTGGAG AATCCCTTTC 180
CTTCCTTTCC CTTTCCAGCT TTTAGAGGCT GCCTGCATTC CTTGGCCTGC AACCCCTTCC 240
TCCACTTTCA AAGCCAGCAC TGGCTGGTCA GGTTTTTCAC AATGCGATCT CTCTGGTTCT 300
GACCCTTCTG CCTCCTCCTT CTTCATTTAA GAACCCTTGT GATTACACTG GGCCCACACC 360
AATAATCCAG GGTAATCTCT CTATTTGCAA GTGAGCTGGT TAGCAACCTT AATTCCATCT 420
GCAGTTTTAA TTCCTCTTTG CCATGTAGCA ACATATTCAT AGGCTCATGC ATTAGGACGT 480
GGACCTCTTT ATTCCACTGT GGACCAATAC TCTGCCTTCC ACACCTAGCC TCTCTTCTGA 540
GTTTTCCAAG GGCCCCCCAT CCTCAGGCAT CCTCAGGCAT AGACAGCCGG CTGGGCCAGA 600
CCACAGTCAG GATGTTCCCG CCACTATCAG AGAGGTCCTT TCTACCTAAG TCCCCTCCCA 660
CCTGCCTGCT CCTCTTTCAG CTCGGTCTGT CCTGGATTCC TCTTCCTTCA TCCTCTGCTC 720
CCAGTCTTAG GTAGAGAAGA GCTGAGCAGG AAGTGCCAGG GGGTGTGGAG ATGGAGGAGG 780
GGGAAGGTAA GGCCTGAGGC ACCAGGGCTC TGGGAGCCCA GGGAGCTGAG GCCTTTCAAT 840
CCAGACACCC TGCACTTCTC TGGCTCTGGG GCCTCTGGGG ACCACACACT CAGCTCCAGG 900
GCTGGAGGGG TGGCCAGCCA AGTATTGGAA CCCTTCTGCT TGTACATCCC TAGCTGCCCT 960
TAACAGCCAC AGTTCACCTG GCCCTTTTCT TGGGTGATGA CAGACTGTCT GCCTTAATTT 1020
ATTCCCTTTC CCCTGTCCCT CCCTAGGCCT CAGGCTGGAA CTTTCAGGAG CTTCCACGGG 1080
AGGCAAGGCC CCAGCCAGGC CTCTGTCCCT GGGCTGCTTG GTGTGGGGAT GGGGGATCCA 1140
GAACCCCAGC AGGAGGGCAG ATGGGGAGCA CAGGGCAGGA GGGGCAGGAC AAAGCCTTTG 1200
GCCCTCAGGG AGGGTGACCA ACTGGCCCTG GTTTGCCTGG GACTTTCCCA GTTTTAGCAC 1260
TGAAAGTCCC AAATCCTGGG AAACTCCTCA GTCCTAAGCA AACTGGAACA GTTGGTCAGC 1320
CTATCTCCAA GCCTTTTGCA CCTCCTAATC 1350