EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-08376 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr2:85146530-85147930 
Target genes
Number: 5             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr2:85147161-85147172GATGAGTCACA-6.14
Foxd3MA0041.1chr2:85147247-85147259GATTGTTTATTT+6.62
HNF4GMA0484.1chr2:85147639-85147654TGGCCTTTGGCCTTG-6.47
HNF4GMA0484.1chr2:85147595-85147610TGGCCTTTGGACTCT-7.58
JUN(var.2)MA0489.1chr2:85147162-85147176ATGAGTCACATCCT-6.21
JUNDMA0491.1chr2:85147161-85147172GATGAGTCACA-6.14
Nr5a2MA0505.1chr2:85147876-85147891GCTGGCCTTGAACTC-8.25
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_10467chr2:85145440-85148104CD19_Primary
SE_14858chr2:85146216-85148097CD4_Memory_Primary_7pool
SE_15828chr2:85146211-85147858CD4_Naive_Primary_7pool
SE_17329chr2:85144702-85148021CD4p_CD25-_CD45RAp_Naive
SE_18307chr2:85145257-85148272CD4p_CD25-_Il17-_PMAstim_Th
SE_19290chr2:85146834-85148007CD4p_CD25-_Il17p_PMAstim_Th17
SE_22056chr2:85146279-85147703CD8_Naive_8pool
SE_24195chr2:85147396-85147781Colon_Crypt_2
SE_27502chr2:85146415-85148139Esophagus
SE_32545chr2:85146405-85147995GM12878
SE_34685chr2:85144533-85148900HeLa
SE_35873chr2:85145245-85148284HMEC
SE_37561chr2:85145355-85148665HSMMtube
SE_39196chr2:85146289-85148051IMR90
SE_43289chr2:85146287-85148018Lung
SE_45342chr2:85146235-85148013NHLF
SE_47378chr2:85146394-85148070Panc1
SE_50337chr2:85146275-85148041Sigmoid_Colon
SE_52528chr2:85146343-85148031Small_Intestine
SE_54030chr2:85146413-85147977Spleen
SE_55507chr2:85147282-85147950Thymus
SE_55909chr2:85146272-85148271u87
SE_57573chr2:85146370-85147966VACO_503
SE_58212chr2:85146543-85147124VACO_9m
SE_58212chr2:85147243-85147947VACO_9m
SE_65145chr2:85146145-85148023NHEK
SE_67823chr2:85146272-85148271u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr28514709385147556
Number: 1             
IDChromosomeStartEnd
GH02I084918chr28514533485148597
Enhancer Sequence
CTGACCTCAG GTAATCCATC CGCCTTGGCC TCCCAAAGTG CTGAGATTAC AGGCGTGGGC 60
CACCATGCCT GGCCAGACAG TCCAATATTT TTAAATCAGC CATAAATCTA TGCACCGAAT 120
AATGTCTCTC TCTCTCTCTC TGACACATAC ACACATACAC ACATGCGCAC GCGTGCACAC 180
CCACACATTG TTACCACTTA GAAGAGTGCC AGGCCCAGAT GGTTTCACAG ACGATTGCTT 240
TCAAAGCTGC AAGAAAGCAA TAACTTCAAT ACCTCAAAAT TTGTTTCAGT AGTTAGAAAA 300
GGACATATGC TTCCTGTGAT GGTTAATTTT AGCTGTCAAC TTGACTTGAT TAAGTAATAC 360
ACTAGTCTCC CCTTATCCAT GGAGGGTATG TTCCAAGATC CCCAGTGGAT GCCTGAAGCC 420
ACACATGTAC CGAACCCTGT ACACACCTAT GATAACGTTT AATTTATAAA TTAGGCACAG 480
TAAGAGATTA ACAACTAATA ATAAAATAGA ACAATTAAAC AGTTGAACAC AAGCACTGTG 540
ATGCTGTGAC AGTCACTCGT AACTGAGATG GCTGCTAAGA GACTAGCTAA CGGGTGAGTA 600
GTGTATACAA CGTGGAAACA CTGGACAAAG GGATGAGTCA CATCCTGGGA GGGACAGAGT 660
GGAATGCCAT GAGATTTCAT CATGTTACAC AGAACGATGA GCCATTTAAA ACTTACGGAT 720
TGTTTATTTC TGGAATTTTT AATTTAATAT TTTCAGACCA AGGTTGACCA GGAGTAACTA 780
AAACTACAGA AAGCAAAACT GAATAAAGTG GGGAGTCGAG AACCTAGAGA GCTGGTAAAG 840
CATTCTTTCT AGGTGTGTCT GTGAGGGTGT TTTCACAGGA GATTGGCATG TGAGTGGGTG 900
GGCTGACTGA GGAAGATCTG CCCTCAGTGT GGGCGGACAA CATCCAATTG GCTGTGGGCC 960
CAGATAGAAC CAAAAGGCAG AGAAAAGGCA AATTCTTTTT TTCTCTCTCC TGAAGCTGGG 1020
CCATCCTTCT TCTTCTGACC TTGGACATCA GAACTGCAGG CTCCCTGGCC TTTGGACTCT 1080
GGGTCTTACA TTAGCAGCCC CCAGGTTCTT GGCCTTTGGC CTTGGACTGA GAATTACACT 1140
ATCAGCTGCC CTGGTTCTGA GACTTTAGGA CTTGAACTGA GCCCCACTGT GGTATTCCAC 1200
GGTCTCCAGC TTACAGACAG TCTGTCGTGG GACTTTTCAC CTCCCTAATC TCATGAGCCA 1260
ATTCCCCTAA TAAATCCCCT CTCATATATC TATATACAGT CGCCCCTCAT ATCTATGGGA 1320
GATGGGTTCC AGGTTATGTT GCCCAGGCTG GCCTTGAACT CTTGGGCTCA AGCTATCCTC 1380
CCATCTCAGC TTCCCAAGTA 1400