EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-27433 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr5:131794780-131796900 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:131796318-131796336GCTTCCTGCCATCCTGCC-6.14
EWSR1-FLI1MA0149.1chr5:131796322-131796340CCTGCCATCCTGCCTTCC-6.76
Klf1MA0493.1chr5:131795063-131795074TGGGTGTGGCC-6.62
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00037chr5:131790656-131796338Adipose_Nuclei
SE_01257chr5:131794641-131795249Adrenal_Gland
SE_09163chr5:131788117-131797621CD14
SE_10340chr5:131790824-131795464CD19_Primary
SE_10915chr5:131787711-131797453CD20
SE_11856chr5:131788689-131797117CD3
SE_13479chr5:131790641-131796411CD34_Primary_RO01536
SE_14495chr5:131789106-131797177CD4_Memory_Primary_7pool
SE_16304chr5:131790613-131795606CD4_Naive_Primary_8pool
SE_16894chr5:131794286-131795229CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131789423-131795425CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131787920-131797394CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131787905-131797327CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131790791-131797009CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131788439-131797324CD56
SE_20775chr5:131790546-131796689CD8_Memory_7pool
SE_21960chr5:131790607-131795345CD8_Naive_8pool
SE_22284chr5:131788012-131797561CD8_primiary
SE_23079chr5:131794575-131796517Colon_Crypt_1
SE_23750chr5:131794696-131796088Colon_Crypt_2
SE_23750chr5:131796561-131796935Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131790957-131797727Duodenum_Smooth_Muscle
SE_26597chr5:131794257-131796075Esophagus
SE_27629chr5:131790763-131801421Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131790670-131796844Fetal_Thymus
SE_31393chr5:131794548-131796995Gastric
SE_37771chr5:131791257-131796632HSMMtube
SE_39368chr5:131791092-131797698Jurkat
SE_40726chr5:131794433-131796690Left_Ventricle
SE_42103chr5:131794463-131796999Lung
SE_43869chr5:131790540-131795910MM1S
SE_50023chr5:131791250-131797789RPMI-8402
SE_50051chr5:131790768-131797132Sigmoid_Colon
SE_52336chr5:131790812-131797015Small_Intestine
SE_53285chr5:131790524-131796944Spleen
SE_55171chr5:131794927-131796428Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131794596-131795860Pancreatic_islets
SE_66244chr5:131791092-131797698Jurkat
SE_67186chr5:131790540-131795910MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131796798131796851
chr5131795517131796169
chr5131795209131795478
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GTCAGGAAGA AGCAATTGGA GCTGGCAGTT AAGAATCTTT AGGAATGTGA CCTCTACTTC 60
AGAAGGGTCC AGGGAGGGCC TGTGGTGTCC ACAGCTGCCA CAGACATTTC CTAACCACAA 120
AAATGGCCCC TTGGTGGTCT CCCCAGAGCT CCAGGCAGTC ATGGGGAGGA AGCGGAGGGC 180
CCCATGCCAG GTACTTCCCA GTTTCTAGGC CAACATGAAT GGGACACAGC TCATATGGGG 240
TTGTGGTTAG ACTGGGGACA GTGGAGCATA TGTTCTGGGG ACCTGGGTGT GGCCAAGGGA 300
GGCCTCCTGT CTGTGGCCTT TGTCCCAGAT TGGAAATCAG CCAGTGGGGC TCTCCTACAT 360
GGGTCCAGGC CTGGCTAGCT CTTGAATTCT GTGCGTTTGC ATGTGGGTCC TTATGCATGC 420
GTCCTAGAGC AGGGTCCCAG GGGGCCACTC CCCCCCCCGA CCCCTTACTC CTCTAAGCTG 480
GGAAACACGT GGCATGAGAG AACACACTGT GGCTTCTAAT GACATCGTGT CTTGATTGCA 540
TCCCCATTGC ATCATCTGGG CTCATCTCAT CCCCACCTCT GGACTGTAAC ATCATCCCAG 600
GGACTGCCGG ACACTCATCT GTGCTCCCCC ACAGAGAGTA TAATGCCATT TGGTAATTCA 660
GTACAGCCTC TTCCAACTTG AGAAAGAAGA TGCATTTCCT TCCCTCAGTC TTGAGCTGTG 720
CAGGTGTCAC GCTGAGCTGC CCTGTGTGGG CTCCATGTTG GCACACATCG GTTGCAAGGG 780
GCTCTGTGTA GTGAGTCTGG AGTTGGACCA CTGGCCAGGC GCTGGGATGC TAGTGCCTGG 840
ACTGAGTGTG CACAGAGGCC CCTCAGGCAG AGCCACAGTG GGCGCTGAAC CTCCTGGTGA 900
AGTTCACCGC AGTAACTAGA GCTCAGTGGG AGGGGCTGGC CTATCAGCAC CTGTCCTGTG 960
TGCTTTTTGA AAAGAGCAGG GTCTACCTTC TGTCAACTGA AGTCCTGCCA GCTGCATGGC 1020
ATGAGATGAG GGACAAAGTG GCACGTGAAC AAAGTTGACA TTTTGGAGGC TGTTAGGCTC 1080
AGAGCCAACC CTGGGCTCCA TGTAGTGCCA TGACTCATGG ATTCAGGCCC ATCTTGGAAA 1140
TTGCTCTGGG CGTAGAGCTC TCATTTCTGA TAGTCCAAGT GCAGATATTG GGGTTCCTCT 1200
AATTGGCCCA AATGGTGGCC TGCACCAACC AGCGACCAGA GTGCTGTCTG AATCTAGAAT 1260
AACAGGAAGA ACACGCCTCC AGCAGTGTAG GAGAGTTCCC CATGCAGTGT GCTTCCCATT 1320
CTTACCAGCA GTTGGTATCT TCTGTCTTTT TCACACTGGC CATCTGAGTC TCATAAGGAG 1380
ACTCCTCTCC TTCCACTGAG CCTGCATCCC AGCCTCTCCC CTTTCTTCAG GGACCTCTCC 1440
CCAGCAATTA CGCCCTTCCA TTCTCTCAAC CAGGGAATCT TCAAACTCTT CTTCTCCACT 1500
GGCTCCTGCT GTGCTCCTGT CTCCATCACC TGTATAATGC TTCCTGCCAT CCTGCCTTCC 1560
CCGTGGAGTA CAGCCATGCT GTCTGCTGCT TACAGCCAAG ATTCTGGAAA GAAATGTCTC 1620
CTTTTTCCTC GTCATCAACC ACTCATTTAT TCAGCAAGTG TTTCTTTTAC ACTTGCCTGT 1680
GCTGGGCATG GCAGCAATGC AGCAGTGAAC AAAACCATCA GCCCTGCTCT CATGCAGCTT 1740
ATAATCAAGT AGAGAGACAG ACATAAATGA TTAATAGATG CTCCTGTAAT GGTGGTTGTG 1800
AGGTGTGCTG CCACAGCCCA GCCACACACG CCAGTTCCCT TCTCTGCACA TGTACATGTC 1860
TGCTCATCCT TCCCACCTGA ACTCATGTGC CACCTCACTT ATGCCCCTTC CCAATGCCGC 1920
ACCCACACAA CAGGGTGTCC CTCTGTGCCC ACAGCAGCCC TTGGGTATAA CTGTTCCCCA 1980
CAGAGGCTGA ACCCCAAGGG CAGAGTCCAG GCCACACTCA CCACGGAGAC CCCTGCCTGG 2040
CACAGAGCCC AGCCCAGCAG AGATGCTCAG AAGATGAATG AAAGTCCCTG CTGAGATTGA 2100
TCCAATCTGT TTGTGAACAT 2120