EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS165-09977 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr3:46990150-46992880 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
POU2F2MA0507.1chr3:46991795-46991808TACATTTGCATTT+6.03
RARA(var.2)MA0730.1chr3:46990879-46990896AGGTCACACAGAGGGCA+6.61
ZfxMA0146.2chr3:46992490-46992504GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00943chr3:46987333-46991985Adrenal_Gland
SE_02008chr3:46987772-46990525Aorta
SE_11155chr3:46963907-46992913CD20
SE_13638chr3:46988105-46991652CD34_Primary_RO01536
SE_14564chr3:46984749-46992585CD4_Memory_Primary_7pool
SE_16650chr3:46987830-46991302CD4_Naive_Primary_8pool
SE_18708chr3:46986099-46991562CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46985017-46993140CD56
SE_22640chr3:46985615-46991406CD8_primiary
SE_23114chr3:46987260-46991352Colon_Crypt_1
SE_23114chr3:46991414-46992102Colon_Crypt_1
SE_23749chr3:46987346-46991294Colon_Crypt_2
SE_23749chr3:46991488-46992032Colon_Crypt_2
SE_26114chr3:46983078-46991394Duodenum_Smooth_Muscle
SE_27142chr3:46983018-46992857Esophagus
SE_28145chr3:46982939-46992085Fetal_Intestine
SE_28630chr3:46982992-46992260Fetal_Intestine_Large
SE_30558chr3:46988988-46991255Fetal_Muscle
SE_31407chr3:46987243-46992180Gastric
SE_32585chr3:46989343-46991413GM12878
SE_38780chr3:46987824-46991550HUVEC
SE_40617chr3:46975387-46993135Left_Ventricle
SE_41619chr3:46988621-46991305LNCaP
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46987822-46991381Pancreas
SE_48306chr3:46987919-46991489Psoas_Muscle
SE_48684chr3:46987782-46991986Right_Atrium
SE_49453chr3:46989698-46991296Right_Ventricle
SE_50160chr3:46987309-46992159Sigmoid_Colon
SE_52388chr3:46987277-46992190Small_Intestine
SE_52388chr3:46992258-46992958Small_Intestine
SE_53507chr3:46987802-46992203Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_64772chr3:46987179-46991025NHEK
SE_65471chr3:46977753-46993036Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34699043746991167
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
AGGAGGGCCC GCTCCACTCA GAAGAGAGGC ACGCTGGGCC CCACCATCCA TATGGCACCT 60
CAAGGGCCAG GCCACGGCAT GCCTAGTGCA GCTCCTCGCC AGGCCCGTCA CACGGCCCTG 120
CCCAGATATC CTCCATGTGT CTGTCAGGAG TGTGGGGAGC CAGCCCAAGT CAACTCTGAT 180
CCTATTCTTG CTGCAAGTGC TCAAGGGAGG CACTACAGAG CTCCTCCAGC AGACTTTATC 240
AGTCGACAAA TACTGACTGG CTCCCCTGTG GTACTCCATG CTGTACTCAG ATACTCCATG 300
CTGGGTACTG AGGAGGAAGA GGAACGAGTA GGCACCTAGT GCCCACAGAG CAGGGCAGGG 360
GTTCTTATCC TCGGTGCACA GATTCCAGAG GTCAATGACC AGACAGAAAC ACAGGCGAGT 420
GTGAGAAGGT GAATCTTAGT GGATGAGAAA TCTGGAGCTC TTCAGATTCT CAAGGGGGTG 480
GTGACCCACA GGGGAAAAGG GAAGGTGTCA ACAGCCAGGG AAGGCAGTGT TTTTTTGGGT 540
GGCATTAAGA GGTGTCTACA GAGGCTTTCC AAAGGAAGTG TCACCTTAAA GGATGAGTGA 600
CAGTGGGGAC AGAGGGACGG AGGGGGAAGA GAGCAGAGGG AACAACCAGA ACCATTAGTA 660
TGCAAAAGGC CCCTCCCACT GCCCTGAGAC TTCACCCACA CTGGCCCCAG CAGGAAATAA 720
CCTCTTGAAA GGTCACACAG AGGGCAGGGC AAAGACCAGT CTCTTCCCCT TCCTTCATAT 780
GCAGCCAGAC TGGACGAGTT CCTCTGGGAA GTCTGGCCTG GCTCCAAACT CCCTCCAGGG 840
TCCTCCCTGT AGGGGCACTG TGGTATGCAG GAAGCCCAGC CTGCAGCCCT GGACTGGGCA 900
GGTGGTGGGA ACATCAGGAC ACACTGCTTA CCAGTGGTGG GACCTCCCTG AGGCTCTGTC 960
TCCTCCCCTG TCAAAGTGGG GCTGGCACTA CTTTAACAGG GGCATGTGAG GATTATACAA 1020
GGCAACTTGG GTCCACCATG TGGTACAGGG TCCCGCATGA CCCTGCACCA TGAAAAACTG 1080
CCTGCTGGCC GGGCACAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA 1140
GGTGGATCAT AAGGTCAGGA GTTCGAGACC AGCCTGGCCA ATATGGTGAA AACCTATCTT 1200
TACTAAAACT ACAAAAATTA GCCGGGCATG GTGGCGGGCG CCTGTAGTCC CAGCTACTCG 1260
GGAGGCTGAG GCAGGAGAAC TGCTCGAACC CAGAGGTAGT GGTTGCAGTG AGCCAAGATT 1320
GCGCTACCAC ACTCCAGCCT GGGTGACAGA GTGAGACTCC ATCTCAAAAA AAAAAAAAAA 1380
AGAAAAGAAA AAAAAACTGC CTGCTGACAT CTTGCAGTGT CCCAAGTCCT GCTGTCCCTC 1440
AGCGATGGGC CTAATTCGAA CCCTGGTTCT TGCTGCATCC CTCTTAGGGA ACCTGATGCT 1500
CCTTCTGTTC TCACCCACCC CTTGCCCTGA CACAAAAACC AAGAAAGCAC TTAACAAGAA 1560
CCCAGGACCC AGCACCCAGG GCCCAGATCC ATGCTGGGAA ACAGAAGGCC TATTAGTATT 1620
AGACCAACCA GAAGAGAAAT TGATCTACAT TTGCATTTTT TTGAGATAGG GTCTCGCTCT 1680
GTTGTCCAGC TGTCCAGGCT GGAATGCATG GTGCAATCAT AGCTTACCAC AGCCTGAAAT 1740
TCCTAGGCTC AAGTAAACCT CCCACCTCAG CCTCCTGCAT AGGAGTAGCT AGGACTACAG 1800
GGGCATGCCA CCATGCACAG CTTTTTTTTT TTTTTTGGGG TAGAGACAGG GTCTAACTAT 1860
ATTGCCAAGG TTGGTTTCGA GCTCCTGGGC TCAAGTAATC CTCCTGCCTT GGCCTCCCAA 1920
AGTGCTGGAT TATAGGCATG AGCCACATGC CCAGCCCATT TTTTAAAATG TAACAACATT 1980
CATGTGAATG GAGCACATTA TCCTTTTCTG AAAGTGCTAC ATTTTTTTGG CTAAGTCTCT 2040
GTATATGCTA AACTTAATTT TTAAAAGTGA GGCTCAAATG GAAATAACCT GTGTCCATAA 2100
ATGGATGAAT GAGTAAGAAA ATTTAGTATA TACACACAAT GAAATACTAT TCAGGCTTCA 2160
AAAAAAAAAG AGGAAATCCT GTCATTTGCA ACAACATGGA CAAATCTGGG GAACATTATG 2220
CTAAGCGAAA TAAGCCAGGC TCAGAAAGAC AAATACTGCA TGATCTCACT TATATGTGGA 2280
ATCTAAAACA GTAGAACTGG CCAGCCACAG TGGCTCACAC CTGTAATCCC AGCATTTCGG 2340
GAGGCCGAGG CGGGTCCCAA CTACCCAGGA GGCTGAGGTG GGAGGATCAA ACAAGGCCAC 2400
GAGGTCAAGG CTGCAGTGAG CTGTAACTGA ACTACTGCAC TCCAGCCTTG GCAACAGAGT 2460
GAGACTCGTA TCTCAAAAAA ATTAAAAATT AAAATAAAAA AATAAAAAGT AGAACTCACC 2520
GAAACAGAGA CTAGATGGGT GGTTACAGAG GCTGGAGTTG CAGGAGAGGT GGAGAAAGTG 2580
AAGATGTTGG GCAAAGGACA CAAAGTTCCA GTTAGGCAGG AGGAGTGTGT TTAAGGGAGC 2640
TACTGCACAG CATGGTGATC GGTTAATAAT AATGTATATT CAAAATTGCT GAGCCTAGAT 2700
TTTAAAGTCT CACCACAAAA AATGTTAAAT 2730