EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS167-03767 
Organism
Homo sapiens 
Tissue/cell
Retina 
Coordinate
chr3:46988730-46991500 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr3:46989860-46989871AGAGATAAGGA-6.02
NR2F1MA0017.2chr3:46989541-46989554CAGAGGTCATGGG+6.22
RARA(var.2)MA0730.1chr3:46990879-46990896AGGTCACACAGAGGGCA+6.61
Number of super-enhancer constituents: 37             
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_23749chr3:46987346-46991294Colon_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_49453chr3:46987803-46989682Right_Ventricle
SE_49453chr3:46989698-46991296Right_Ventricle
SE_50160chr3:46987309-46992159Sigmoid_Colon
SE_52388chr3:46987277-46992190Small_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: 4             
ChromosomeStartEnd
chr34698953346989702
chr34699043746991167
chr34698877546989017
chr34698973646990203
Number: 1             
IDChromosomeStartEnd
GH03I046941chr34698304846992889
Enhancer Sequence
GGGAAAAAAG CAAAAGAGAT GGGCACATAG TGCCTGAAGG TGACAGGAAG AGACAGACAA 60
TGCTGGGGCA AACTTGGCAG GCTCCCCAGT GTCACCTTGT GCCCATCCTC AGGGCCACTG 120
CAGCCCCATG CCGGGGTGGA GGGACTTCCT GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT 180
CCAAGGGCAC TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG ACTCACCCTG AAGATGGAGT 240
GATAAGAAGT GAGCTGAACA CCACCATGCC TGGGACCAGA AACTGCACAG ATCTCTACTG 300
CCCAGAGACT GGCAGGGGGA AAGGGGGAGA GACTCTGCTT CTCCTGGGCA GGCTGAGATC 360
TCGTCAGGCT GCAGAGCTCC TCACTCTGGG TCCCCTGCAC TCAATGTGCT GCTAGGATGA 420
CTTGGTCCGA GTATCCACTC TATCTGCTGA CCAGACCAAG AGTTCCTAGA GGGCAGACGT 480
TTGTTGTACC AGTTTGCACC CACAGGCCTG ACACCAACTA CAGCAGGCAC AGCACTGTGG 540
TAGAGGAGTG CACAGGAGCG GGGAAATCCC AGCTCCATTT CATCTTGGCT GTGTGACCTT 600
GGGCAAGTTA TATGACCTGT CTGGCCTCAG TTTCCTCATC TACAAAAATG AGGATAATCA 660
TACTGACATC ATATCACCAT TACAAGGAAA TGATGAAGGA GAAAAGCCTG CAGCTTAGGG 720
AGCCTGAAGA ACAGGGAGAA TCAGGCCAGG GCAGGAAGGA AAGGGCTGCA GAAAAGCCAG 780
CGGGGCACAG GCCCAGAACG GTGTGCCTCT GCAGAGGTCA TGGGAAGCTC CCATGCCCAT 840
CATCCTTATC AGATGTTCTC AGCAATCCTG TAAGCAGACA GGGCAGTGTT GTAATACCTG 900
CTTCACCAAG ACATTAGGAG ATGACGTCAG ATGATCTGTG CAGTGTAGAC AGATCTGATT 960
CCCCATTCAG TGCTTCACCA AGAGTCAGCA GGAACAGGTG GTGACTACCA TCCAAGAGGC 1020
TGGGATTAGC TAAGAGCCAC TGCTCTCCTG TGGGTTCATG TGTTCCCTAA AGGCTTCTGA 1080
GCAGAGCAAG AACAAAGCGC TGAGCGGGAG GCTGGGAGAA CAGCGAGGCT AGAGATAAGG 1140
ACTGGAGATA AGGACGGGAA CTAGGTCAAC AGCGGTGGAC TAGAACAAGG AGGTGCCTCA 1200
ACGCTGTGGG GAGACAGGGA GGAGCAGAAA CAACTGAGGT TCTGCTGGTG ACTCACTGGG 1260
GGAAGGAAGG CGCCTTTGAC AAAAAGGTGG TGGCACTTAG GGGACAAAGA GAAAGGGTGT 1320
GGCAGCCTTC AGGCATTCTA ACGGTGAGGC TTGACACCCA AGGCCTGACG AAGGTTGGTG 1380
CCAAGGGATA GCACCTGTCA AGGTGCCCTC AGCGGTGGAA AGGAGGGCCC GCTCCACTCA 1440
GAAGAGAGGC ACGCTGGGCC CCACCATCCA TATGGCACCT CAAGGGCCAG GCCACGGCAT 1500
GCCTAGTGCA GCTCCTCGCC AGGCCCGTCA CACGGCCCTG CCCAGATATC CTCCATGTGT 1560
CTGTCAGGAG TGTGGGGAGC CAGCCCAAGT CAACTCTGAT CCTATTCTTG CTGCAAGTGC 1620
TCAAGGGAGG CACTACAGAG CTCCTCCAGC AGACTTTATC AGTCGACAAA TACTGACTGG 1680
CTCCCCTGTG GTACTCCATG CTGTACTCAG ATACTCCATG CTGGGTACTG AGGAGGAAGA 1740
GGAACGAGTA GGCACCTAGT GCCCACAGAG CAGGGCAGGG GTTCTTATCC TCGGTGCACA 1800
GATTCCAGAG GTCAATGACC AGACAGAAAC ACAGGCGAGT GTGAGAAGGT GAATCTTAGT 1860
GGATGAGAAA TCTGGAGCTC TTCAGATTCT CAAGGGGGTG GTGACCCACA GGGGAAAAGG 1920
GAAGGTGTCA ACAGCCAGGG AAGGCAGTGT TTTTTTGGGT GGCATTAAGA GGTGTCTACA 1980
GAGGCTTTCC AAAGGAAGTG TCACCTTAAA GGATGAGTGA CAGTGGGGAC AGAGGGACGG 2040
AGGGGGAAGA GAGCAGAGGG AACAACCAGA ACCATTAGTA TGCAAAAGGC CCCTCCCACT 2100
GCCCTGAGAC TTCACCCACA CTGGCCCCAG CAGGAAATAA CCTCTTGAAA GGTCACACAG 2160
AGGGCAGGGC AAAGACCAGT CTCTTCCCCT TCCTTCATAT GCAGCCAGAC TGGACGAGTT 2220
CCTCTGGGAA GTCTGGCCTG GCTCCAAACT CCCTCCAGGG TCCTCCCTGT AGGGGCACTG 2280
TGGTATGCAG GAAGCCCAGC CTGCAGCCCT GGACTGGGCA GGTGGTGGGA ACATCAGGAC 2340
ACACTGCTTA CCAGTGGTGG GACCTCCCTG AGGCTCTGTC TCCTCCCCTG TCAAAGTGGG 2400
GCTGGCACTA CTTTAACAGG GGCATGTGAG GATTATACAA GGCAACTTGG GTCCACCATG 2460
TGGTACAGGG TCCCGCATGA CCCTGCACCA TGAAAAACTG CCTGCTGGCC GGGCACAGTG 2520
GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA GGTGGATCAT AAGGTCAGGA 2580
GTTCGAGACC AGCCTGGCCA ATATGGTGAA AACCTATCTT TACTAAAACT ACAAAAATTA 2640
GCCGGGCATG GTGGCGGGCG CCTGTAGTCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAC 2700
TGCTCGAACC CAGAGGTAGT GGTTGCAGTG AGCCAAGATT GCGCTACCAC ACTCCAGCCT 2760
GGGTGACAGA 2770